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Sign in to claim this brandBiomet Uk Ltd
US
Last updated May 24, 2026
What Biomet Uk Ltd makes
Biomet UK Ltd manufactures unicondylar knee prostheses, trial components for knee and hip implants (including tibia, femur, and femoral head), reusable surgical instruments such as templates and probes, and orthopaedic tools like bone-reamers and implant inserters/extractors. Their portfolio also includes modular hip systems and gap gauges for knee alignment, designed for use in orthopaedic and ENT surgeries.
The company’s devices are classified under FDA categories Class I, II, and III, with listings in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates under US regulatory oversight, adhering to applicable medical device compliance standards.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Biomet UK Ltd manufacture?
Biomet UK Ltd specializes in orthopaedic and reusable surgical devices. Their portfolio includes unicondylar knee prostheses, trial components for knee and hip implants (such as tibia, femur, and femoral head trials), reusable surgical instruments like templates and probes, and orthopaedic tools such as bone-reamers and implant inserters/extractors. They also produce modular hip systems and knee alignment gauges, primarily for orthopaedic and ENT surgical procedures.
Where is Biomet UK Ltd based, and under which regulatory framework do they operate?
Biomet UK Ltd is based in the United States. Their devices fall under FDA regulatory oversight, meaning they must comply with U.S. medical device regulations, including classification under FDA categories such as Class I, II, or III. This framework ensures their products meet safety and performance standards before entering the market.
Which regulatory registries or databases list Biomet UK Ltd’s devices?
Biomet UK Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution and use, ensuring transparency and traceability for regulatory and clinical purposes.
How are Biomet UK Ltd’s devices classified by the FDA?
Biomet UK Ltd’s devices are classified under three FDA categories: Class I (generally low-risk devices), Class II (devices requiring special controls to ensure safety and effectiveness), and Class III (high-risk devices requiring premarket approval). Classification depends on factors like intended use, risk level, and potential impact on patient safety, with stricter oversight for higher-risk devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- zimmerbiomet.com
- —
- —
- [email protected]
- Phone
- +1(800)348-9500
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 219322575
Catalogue (1179)
Page 16 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hiploc System | 190103 | FDA UDI | Class II | Active |
| Oxford Unicompartmental Knee Phase 3intramedullary Awl | 32-420540 | FDA UDI | Class I | Active |
| Neck Resection Retractor | 31-555516 | FDA UDI | Class I | Active |
| Recap Hip Instrumentation | 31-600385 | FDA UDI | Class I | Active |
| Modular Acetabular Grater Reamershell 66mm | 29-476066 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 161471 | FDA UDI | Class III | Active |
| Bi-Metric Provisional | 31-473566 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 154613 | FDA UDI | Class III | Active |
| Oxford Partial Knee System | 159569 | FDA UDI | Class III | Active |
| BIOLOX® delta Modular Ceramic Head | 650-1162 | FDA UDI | Class II | Active |
| Hiploc Instrumentation | 470014 | FDA UDI | Class I | Active |
| Ringloc + Instrumentation | 31-400627 | FDA UDI | Class I | Active |
| Oxford Uni Knee System | 32-422843 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 154776 | FDA UDI | Class III | Active |
| Oxford Uni Knee System | 32-422818 | FDA UDI | Class I | Active |
| Asi Instrumentsmedial Calcar Style Retractor | 110028568 | FDA UDI | Class I | Active |
| Oxford® Partial Knee System | 166570 | FDA UDI | Class III | Active |
| Oxford Partial Knee System | 160792 | FDA UDI | Class III | Active |
| Ringloc® Acetabular Provisional | 31-423711 | FDA UDI | Class I | Active |
| Oxford Unicompartmental Knee Phase 3femoral Drill Guide | 32-420322 | FDA UDI | Class I | Active |
| Recap Hip Instrumentation | 31-500956 | FDA UDI | Class I | Active |
| Biodrive Screw System | 35-000229 | FDA UDI | Class I | Active |
| Magnum Instrumentation | 31-141079 | FDA UDI | Class I | Active |
| M2a 38mm | 31-103616 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 154320 | FDA UDI | Class II | Active |
| Oxford Partial Knee System | 32-420821 | FDA UDI | Class III | Active |
| Agc V2 Millennium Instrument | 32-468456 | FDA UDI | Class I | Active |
| Recap/Magnum Instrumentation | 31-158946 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 159595 | FDA UDI | Class III | Active |
| Maxim Knee System | 32-345384 | FDA UDI | Class I | Active |
| Bi-Metric Rasp/Provisional | 31-473612 | FDA UDI | Class I | Active |
| Oxford Unicompartmental Knee Phase 3gap Gauge Size 6 & 7 | 32-420395 | FDA UDI | Class I | Active |
| Maxim Knee System | 32-345341 | FDA UDI | Class I | Active |
| Ringloc Acetabular Provisional | 31-423717 | FDA UDI | Class I | Active |
| Oxford Unicompartmental Knee Phase 3femoral Drill Guide | 32-421060 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 32-422702 | FDA UDI | Class III | Active |
| Oxford Partial Knee System | 32-421067 | FDA UDI | Class III | Active |
| Oxford Partial Knee System | 159571 | FDA UDI | Class III | Active |
| Recap/Magnum Hip Instrumentation | 31-141042 | FDA UDI | Class I | Active |
| Ringloc® Acetabular Provisional | 31-423737 | FDA UDI | Class I | Active |
| Agc Intramedullary Angle Guide | 32-467604 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 154608 | FDA UDI | Class III | Active |
| Agc Revision Knee | 154537 | FDA UDI | Class II | Active |
| Ringloc Acetabular Provisional | 31-423708 | FDA UDI | Class I | Active |
| Oxford Partial Knee System | 154612 | FDA UDI | Class III | Active |
| Oxford® Partial Knee System | 32-422862 | FDA UDI | Class III | Active |
| Oxford Unicompartmental Knee Phase 3spherical Cutter | 32-420330 | FDA UDI | Class I | Active |
| Agc Anatomic | 32-467608 | FDA UDI | Class I | Active |
| BIOLOX® delta Option | 650-1058 | FDA UDI | Class II | Active |
| Agc Total Knee Instrumentationpremier Contour Block | 32-401300 | FDA UDI | Class I | Unknown |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Biomet Uk Ltd. BRIDGEND · GB FEI 3002806535