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Should You Open an On-Site Dental Laboratory in your Dental Pracice? A Practical UK Guide

7/27/2026

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The idea of having an on-site dental laboratory is attractive. Cases could be completed faster, communication with the technician would become easier, shade consultations could happen in the practice and urgent adjustments might be dealt with immediately.

On paper, it sounds like greater control, shorter turnaround times and lower laboratory bills.

In reality, an on-site dental laboratory is not simply a spare surgery with a technician, a workbench and a polishing motor. It is a medical-device manufacturing environment with its own infrastructure, equipment, staffing, health and safety responsibilities, quality systems, regulatory obligations and ongoing costs.

At Bremadent Dental Laboratory, dentists regularly ask us whether they should create their own laboratory. Our answer is never automatically yes or no. It depends on the type of work, the volume available, the skill mix required and whether the practice genuinely wants to operate a manufacturing department alongside its clinical business.

Before committing valuable space and capital, practice owners need to understand what running a dental laboratory actually involves.
First Decide What the Laboratory Will Actually Manufacture
There is a substantial difference between an area used for simple repairs or model production and a full-service laboratory manufacturing crowns, bridges, dentures, splints and implant restorations.
Before designing the room or purchasing equipment, define the proposed scope:
  • Will the laboratory only pour impressions and manufacture models?
  • Will it produce temporary or definitive restorations?
  • Will it manufacture crowns, bridges or implant-supported work?
  • Will it process acrylic dentures, additions and relines?
  • Will it work with cobalt chrome, titanium or other metals?
  • Will it produce 3D-printed models, splints, dentures or permanent devices?
  • Will it manufacture for one practice or supply other practices?
  • Will it employ one general technician or several specialist technicians?

Every additional service introduces another workflow, material, skill requirement and potential risk.

A laboratory making study models has very different requirements from one processing acrylic resin, grinding zirconia, firing ceramics and handling flammable solvents. The production plan should determine the infrastructure, not the other way around.

Why Case Volume Determines Whether an On-Site Laboratory Works
Commercial dental laboratories operate through consolidated volume. Equipment, technicians and departments are shared across cases arriving from multiple dental practices.

One scanner can process numerous cases. A furnace can fire several compatible restorations during the same cycle. Multiple units can be designed, milled, cast or finished together. Specialist technicians can concentrate on the stages in which they are most productive.

A single dental practice may not generate enough consistent work to achieve the same efficiency.

Consider a porcelain-bonded crown with an external laboratory price of approximately £45. Its manufacturing journey may include:
  • Receiving and disinfecting the impression or accepting the digital scan
  • Casting and preparing the working model
  • Articulating the case
  • Preparing the margins
  • Waxing or digitally designing the coping
  • Casting, milling or producing the metal substructure
  • Finishing and checking the metalwork
  • Applying opaque and ceramic
  • Completing multiple furnace cycles
  • Contouring, staining and glazing
  • Polishing, quality control and documentation

The complete production journey can span seven or eight working hours, sometimes longer. This includes manufacturing stages, setting periods, cooling periods, furnace cycles and movement between departments. It does not necessarily mean that one technician spends eight continuous hands-on hours making one crown.

That distinction is central to the economics. Commercial laboratories can batch compatible stages and keep technicians and equipment productive across multiple cases. An on-site technician with only one crown to manufacture does not have that same volume advantage.

A Practical £45 Crown Cost Example
Imagine a practice employing one dental technician at a salary of £32,000 per year.
For illustration, once employer’s National Insurance, workplace pension contributions, holiday entitlement and other employment costs are considered, the direct annual employment cost could move towards approximately £38,000 to £42,000 before the practice pays for a laboratory room, materials or machinery.

If the technician works approximately 220 productive days per year, the employment cost alone could be around £173 to £191 per available working day.

Now assume the technician produces only one £45-equivalent porcelain-bonded crown that day.

The practice has avoided a £45 external invoice, but it may have incurred:
  • Approximately £173 to £191 in employment cost
  • The alloy, ceramic, investment, burs and consumables
  • Electricity for the furnace, compressor, extraction and other equipment
  • Equipment servicing and calibration
  • Software and licensing costs
  • Depreciation or finance payments
  • Waste disposal and compliance costs
  • Management and administrative time
  • The opportunity cost of the laboratory room

The true internal cost of that crown could therefore be several times greater than the external laboratory fee. If ten suitable units move through production together, the economics begin to change because labour, equipment and overheads are spread across more output. However, the practice must be confident that sufficient work will arrive consistently, not merely during an unusually busy month.

A technician’s salary remains payable when dentists are on holiday, patients cancel, cases are delayed or a machine stops working. External laboratory costs normally rise and fall with the number of cases ordered. An in-house laboratory turns much of that variable cost into a fixed overhead.

How Much Do UK Dental Practices Spend on Laboratory Work?
There is no universal percentage because laboratory expenditure depends heavily on treatment mix.

Specialist dental accounting guidance commonly places laboratory fees at approximately 8 to 15 per cent of practice turnover. A practice delivering significant prosthodontic, implant or cosmetic treatment may sit towards the higher end or above it. A practice focused heavily on examinations, hygiene and direct restorations may sit considerably lower.

Christie & Co’s Dental Market Review 2024 reported that laboratory and material expenditure combined represented approximately 15 per cent of practice costs. Importantly, this figure combines laboratory and materials. It should not be interpreted as laboratory fees alone or automatically described as 15 per cent of turnover.

Before considering an on-site laboratory, review at least 12 months of data:
  • Total external laboratory expenditure
  • Laboratory expenditure as a percentage of turnover
  • Number of units purchased each month
  • Spend by product category
  • Average laboratory fee per completed treatment
  • Remake, adjustment and cancellation rates
  • Monthly peaks and troughs in case volume
  • Clinical revenue generated from each laboratory-based treatment

A high external laboratory bill does not automatically justify bringing production in-house. It may simply show that the practice is carrying out a profitable volume of restorative treatment.

The proper comparison is between the external fee and the fully loaded internal manufacturing cost, including the value of the space occupied.

The Infrastructure Required for an On-Site Dental Laboratory
A dental laboratory fit-out should be planned by competent contractors who understand the machinery, substances and manufacturing processes involved.

Depending on the intended work, the infrastructure may include:
  • Dedicated electrical circuits for furnaces, mills, printers, compressors and extraction
  • Correctly positioned sockets and isolation switches
  • CAD Equipment 
  • Computers for CAD
  • CAM Milling units 
  • 3D Printers 
  • Vaccum Mixers
  • Computer system for data entry
  • Network infrastructure 
  • Computer Security 
  • Laboratory CRM software for management of cases
  • Timers where suitable for controlled equipment shutdown
  • Compressed-air lines with filtration, drainage and pressure regulation
  • Gas lines installed and tested by appropriately qualified engineers
  • Flashback protection and secure cylinder storage where applicable
  • Hot and cold water supplies
  • Suitable backflow protection
  • Dedicated plaster sinks and plaster traps
  • Drainage designed for the production environment
  • Local exhaust ventilation at grinding, trimming, polishing and blasting points
  • General ventilation and temperature control
  • Task lighting and colour-controlled lighting for shade work
  • Fire alarms, smoke detection and appropriate extinguishing equipment
  • Secure storage for chemicals, resins and flammable liquids
  • Segregated clean and contaminated areas
  • Washable work surfaces
  • Adequate space around machinery for safe operation and maintenance

Domestic extension leads, improvised extraction and ordinary sinks are not suitable substitutes for correctly planned laboratory infrastructure.

The room must also be large enough to separate incompatible processes. A model arriving from the mouth should not be handled beside a finished crown that has completed final cleaning and quality control.

COSHH Is a Working System, Not a Folder on a Shelf
The Control of Substances Hazardous to Health Regulations require employers to assess and control exposure to substances that may harm employees.

Dental laboratories may use or generate:
  • Acrylic monomer containing methyl methacrylate
  • Photopolymer printing resins
  • Isopropyl alcohol and other solvents
  • Ceramic, zirconia and gypsum dust
  • Investment material dust
  • Metal and alloy particles
  • Cobalt-chromium dust
  • Cleaning and disinfection chemicals
  • Bonding agents, primers and opaques
  • Compressed gases
  • Fumes from heating or processing materials

A safety data sheet is not itself a COSHH assessment. It describes the substance, but the practice must assess how it is stored, mixed, used, cleaned and disposed of within its specific workflow.

A suitable COSHH system should include:
  • A complete inventory of substances and dust-producing processes
  • Current safety data sheets
  • Task-specific COSHH assessments
  • Identified exposure routes, including inhalation, skin contact and eye contact
  • Storage and quantity controls
  • Suitable local exhaust ventilation
  • Spill and emergency procedures
  • Staff instruction and documented training
  • Appropriate gloves, eye protection and protective clothing
  • Respiratory protective equipment where other controls are insufficient
  • Face-fit testing for tight-fitting respiratory protection
  • Health surveillance where the assessment identifies a need
  • Scheduled review after material, equipment or process changes

Personal protective equipment should be the final layer of protection, not the first response to poor extraction. If dust is escaping across the room, handing the technician a disposable mask does not fix the underlying problem.

Dust Control and Local Exhaust Ventilation
Grinding zirconia, acrylic, gypsum, ceramic, investment and metal can release fine airborne contaminants. Some particles may remain suspended after the visible dust has settled.

Local exhaust ventilation should capture contaminants close to where they are generated. General room ventilation does not provide the same control.

The laboratory should consider extraction at:
  • Model trimming stations
  • Polishing lathes
  • Acrylic finishing areas
  • Sandblasting units
  • Metal finishing benches
  • Zirconia and ceramic grinding points
  • Powder-handling and investment areas

Under COSHH, control measures must be maintained in an efficient state and working order. The Health and Safety Executive states that most local exhaust ventilation systems require thorough examination and testing at least every 14 months, although some processes may require more frequent checks.

The laboratory should also carry out routine user checks. Waiting 14 months to discover that an extraction filter has been blocked for half a year is not an effective control system.

Plaster Sinks, Gypsum and Dental Laboratory Waste
Gypsum plaster should never simply be washed into an ordinary sink. It can settle, solidify and block internal drainage and external pipework.

A plaster department normally requires:
  • A dedicated plaster sink
  • An appropriate plaster trap or settlement unit
  • Safe storage for bags of dental stone
  • Controlled mixing to minimise dust
  • A cleaning schedule for sinks and traps
  • Separate containers for solid gypsum waste
  • Collection through an authorised waste contractor
  • Waste-transfer documentation

It is important to classify gypsum correctly. Most non-infectious dental plaster waste is classified as non-hazardous healthcare waste, not hazardous waste. However, it still requires segregation and must not be treated as ordinary mixed waste without checking the permitted disposal route.

Gypsum can generate hydrogen sulphide gas if disposed of in landfill alongside biodegradable waste. This is one reason gypsum-containing waste needs to be kept separate and handled through an appropriate waste stream.

If plaster is contaminated with infectious material or hazardous chemicals, its classification and disposal requirements may change. The practice should not guess. Its waste contractor should confirm the correct waste description, classification code, container and disposal route.

Hazardous Waste Must Be Classified Before Disposal
A dental laboratory can produce several waste streams with different requirements. These may include:
  • Non-infectious gypsum and plaster waste
  • Infectious or clinically contaminated waste
  • Used acrylic and resin containers
  • Uncured photopolymer resin
  • Resin-contaminated wipes and gloves
  • Contaminated isopropyl alcohol
  • Solvents and chemical residues
  • Metal and alloy waste
  • Used burs and sharps
  • Packaging and ordinary municipal waste
  • Waste electrical and electronic equipment

Not every laboratory material is automatically hazardous, and not everything can go into general waste. Classification depends on the substance, contamination and hazardous properties.

Uncured printing resin should not be poured into the sink. Contaminated isopropyl alcohol should not be tipped down the drain simply because it looks clear. Empty chemical containers may also retain hazardous residues.

A suitable waste-management system should confirm:
  • What waste the laboratory produces
  • Whether each stream is hazardous, non-hazardous, clinical or offensive
  • The correct waste classification codes
  • Which containers must be used
  • Where waste will be stored securely
  • How incompatible materials will be separated
  • Which authorised carrier will collect it
  • Which authorised facility receives it
  • Which transfer or consignment documents must be retained

The practice remains responsible for its waste even after it leaves the premises. Using an unverified person with a van does not transfer the duty of care.

Cross-Infection Control Must Extend into the Laboratory
Items entering a dental laboratory may have been in direct contact with saliva, blood or oral tissues. This includes impressions, dentures, bite registrations, implant components and appliances requiring repair.

Cross-infection control must therefore form part of the laboratory design and workflow from the beginning.

The laboratory should establish a clear contaminated-to-clean pathway
  • Receive cases into a designated contaminated area
  • Confirm whether disinfection has already been completed
  • Disinfect incoming items using a material-compatible and validated method
  • Record the disinfection status
  • Use dedicated containers and equipment for contaminated work
  • Clean and disinfect reusable transport boxes
  • Prevent contaminated items entering clean manufacturing areas
  • Clean finished appliances appropriately before dispatch or fitting
  • Label outgoing work with its decontamination status
  • Train every relevant employee in the agreed procedure

A note saying “disinfected” is only meaningful if the practice knows what was used, at what concentration, for how long and whether the method is compatible with the material.

Overexposure can damage impressions and affect accuracy. Underexposure may fail to achieve effective disinfection. The correct method should follow the disinfectant and material manufacturers’ instructions.

Repairs and additions require particular attention because an appliance that looks clean may still be contaminated. Polishing a returned denture without proper decontamination can spread biological contamination across pumice, brushes, polishing lathes, worktops and staff hands.

Pumice systems and polishing equipment need documented controls. Single-use or appropriately managed materials, routine cleaning and separation between incoming and finished work help reduce cross-contamination.

Digital workflows reduce the movement of physical impressions, but they do not remove infection-control responsibilities. Scanner tips, implant components, try-ins, dentures and printed appliances still require appropriate cleaning, disinfection or sterilisation according to their intended use and manufacturer’s instructions.

The Medical-Device Regulations Still Apply On Site
Crowns, bridges, dentures, splints and many other dental appliances are custom-made medical devices.
In Great Britain, the applicable framework includes the UK Medical Devices Regulations 2002, as amended. The former Medical Devices Directive may still appear in older laboratory documentation, but a new facility should follow the requirements applying to its current activities and location.

Responsibilities may include:
  • Manufacturing from an appropriate written prescription
  • Identifying who is the legal manufacturer
  • Meeting applicable safety and performance requirements
  • Producing the required custom-made device documentation
  • Maintaining material and batch traceability
  • Keeping manufacturing and quality records
  • Managing complaints, remakes and incidents
  • Maintaining appropriate post-market surveillance
  • Determining the correct MHRA registration position

Current MHRA guidance distinguishes between devices placed on the market and devices only put into service by the same organisation. A practice manufacturing solely for its own patients may have a different registration position from a laboratory supplying separate businesses.

That distinction should be confirmed before manufacturing begins. “It is only for our own patients” is not a complete regulatory strategy.

GDC Registration and Technical Competence
Dental technicians are registered dental care professionals. Any technician undertaking regulated dental technology work should be registered with the General Dental Council and work within their training, competence and scope of practice.

One technician may be excellent at removable prosthetics but have limited experience in ceramics. Another may be highly skilled in CAD design but unable to process dentures or undertake complex implant work.

Before employing an on-site technician, establish:
  • Which devices they are competent to manufacture
  • Which production stages must remain external
  • How competency will be assessed
  • Who will complete final quality control
  • How continuing professional development will be supported
  • Who covers holidays and sickness
  • What happens if the technician leaves
  • Who manages regulatory and quality documentation

One technician can become a significant single point of failure. A robust external laboratory relationship is still needed for specialist work, overflow and business continuity.

Fire, Electrical and Equipment Safety
A dental laboratory may contain furnaces, compressors, gas, solvents, resins and machinery operating at high temperatures or speeds. These hazards must be included within the practice’s fire and workplace risk assessments.

Controls may include:
  • Suitable fire detection and alarm arrangements
  • Appropriate extinguishers selected through a competent fire-risk assessment
  • Secure storage for flammable substances
  • Machinery guarding
  • Emergency isolation points
  • Compressor and pressure-system assessments
  • Planned equipment servicing
  • Documented staff training
  • End-of-day shutdown checks
  • Spill procedures and evacuation arrangements

Electrical equipment must be maintained so it remains safe. Portable appliance testing may form part of the maintenance system, but UK law does not require every appliance to be tested annually. The inspection and testing frequency should be based on risk and determined by a competent person.

Timers can assist with selected equipment and shutdown routines, but they must not override manufacturer instructions or replace proper isolation and staff checks.

GDPR, the ICO and Digital Case Information
Laboratory prescriptions, intraoral scans, photographs and case discussions can contain personal and health information.

A practice should establish:
  • Who is acting as the data controller
  • Who can access laboratory records
  • How digital files are transferred securely
  • Where scans and photographs are stored
  • How access and amendments are logged
  • How long records will be retained
  • How backups are managed
  • How a data breach will be handled
  • Whether an ICO data-protection fee is payable
  • How old computers and storage devices will be securely disposed of
Personal messaging accounts and uncontrolled file-sharing links are not substitutes for an information-governance system.

DAMAS, the DLA and a Working Quality System
DAMAS is the Dental Appliance Manufacturers Audit Scheme. It provides a dental-laboratory-specific quality framework covering areas such as manufacturing controls, traceability, infection control and documentation.

DAMAS certification is not automatically a legal requirement for every on-site laboratory. However, the disciplines within a structured quality system are extremely valuable.

The Dental Laboratories Association provides representation and industry support. Membership can be beneficial, but DLA membership does not replace GDC registration, MHRA responsibilities, COSHH compliance or a proper quality-management system.

A working system should cover:
  • Prescription acceptance and case booking
  • Cross-infection control
  • Material and batch traceability
  • Equipment maintenance and calibration
  • Manufacturing-stage checks
  • Final quality control
  • Non-conforming work and remakes
  • Complaints and incident management
  • Product recall procedures
  • Staff training and competency
  • Waste classification and disposal

A folder containing generic policies is not evidence of control. The documented process must match what actually happens at the bench.

When an On-Site Laboratory Can Make Commercial Sense
An on-site laboratory can succeed where there is sufficient, predictable volume and a clearly defined purpose.
It may be viable when:
  • Several clinicians generate consistent daily laboratory work
  • The practice delivers significant implant, prosthodontic or same-day treatment
  • Immediate technician involvement materially improves clinical outcomes
  • The initial manufacturing scope is controlled
  • The room is not more valuable as a revenue-generating surgery
  • Recruitment and technical cover are realistic
  • The financial model includes every overhead
  • Compliance and quality responsibilities have named owners

For many practices, a hybrid model is more practical. Scanning, shade-taking, minor adjustments or selected same-day procedures may remain on site, while complex manufacturing is completed by a commercial dental laboratory.
This provides control where proximity adds value without forcing the practice to reproduce an entire manufacturing business.

The Final Feasibility Checklist

Before converting a room or signing an equipment agreement, answer these questions:
  • What exactly will we manufacture?
  • How many suitable units do we produce every week?
  • What is our present external cost per unit?
  • What is the fully loaded internal cost per unit?
  • What happens if volume falls by 25 per cent?
  • What clinical income will we sacrifice by using the room?
  • Who is legally responsible as the manufacturer?
  • Who manages COSHH and cross-infection control?
  • How will every waste stream be classified and collected?
  • Who covers technician absence and equipment failure?
  • Which cases will still require external support?
  • Will the project improve care, or merely move one invoice into several overhead accounts?

If the financial case only works when the technician is continuously productive, every machine remains operational and every dentist supplies the predicted volume, there is not enough protection against normal business variation.

Why a Commercial Dental Laboratory Often Remains the Better Option
A commercial dental laboratory spreads specialist labour, equipment and compliance costs across work from many practices. The practice pays for the required output without carrying the entire manufacturing infrastructure.

Working with Bremadent Dental Laboratory provides access to:
  • Multiple technical departments and skill sets
  • Established analogue and digital workflows
  • Scalable production capacity
  • Defined cross-infection procedures
  • Material and case traceability
  • Quality-control systems
  • Cover during holidays, sickness and changes in demand
  • Support with prescriptions, case planning and problem solving
  • Costs linked more closely to the volume ordered

The purpose of this guide is not to discourage practices from investing in technology. An on-site laboratory can work extremely well when the demand, infrastructure and management systems genuinely support it.

However, owning the manufacturing process only creates control when the practice also owns the expertise, capacity, compliance and commercial discipline required to run it properly. Otherwise, it may acquire a laboratory room while also inheriting an expensive second business.

For many dentists, the most effective laboratory is not necessarily the one located down the corridor. It is the one with the people, systems, equipment and volume to deliver consistent work every day.

We provide a trusted laboratory service delivering consistent quality, saving chairside time, and supporting predictable patient outcomes.

If you don't want the head ache, then please get in touch:

📞: 0208 520 8528

 
📧: [email protected] 

📍: 25A St James Street, London, E17 7PJ
 
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    Clinical Dental Technician Kash Qureshi - Bremadent Dental Laboratory & Swissedent Denture ClinicKash Qureshi - Managing Director, Clinical Dental Technician
    About the author:
    Kash Qureshi is a Clinical Dental Technician (Denturist) in the U.K who oversees and quality controls over 3000+ fixed and removable prosthesis including implant cases from a clinical and technical aspect monthly at Bremadent Dental Laboratory & Swissedent Denture Clinic in London.
    www.swissedent.co.uk  www.bremadent.co.uk [email protected]


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