Biomet UK Ltd
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Biomet UK Ltd is a medical device manufacturer, with 1,354 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class I, III and II; EU Class I) and 33 FDA recalls as of 12 Nov 2026.
- Devices
- 1,354
- FDA recalls
- 33
Registry facts
- Registries
- FDA GUDID 1,312
- EUDAMED 236
- FDA 510(k) 3
- Device classes
- FDA Class I 799
- FDA Class III 402
- FDA Class II 85
- EU Class I 33
- EU Class III 20
- EU Class IIa 15
- Top EMDN categories
- FDA recalls
- Sites and related companies
- Biomet UK Ltd. United Kingdom
- Identifiers
- DUNS 219322575
At a glance
Market reach
- United States
- FDA recalls
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.
Catalogue
Search and filter all 1,354 devicesShowing 1-50 of 1,354
Company details
- DUNS number
- 219322575
- Phone
- +1(800)348-9500
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 4
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2018
- 9 Aug 2018 Z-3261-2018 Class II Terminated HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
- 9 Aug 2018 Z-3262-2018 Class II Terminated HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
- 9 Aug 2018 Z-3263-2018 Class II Terminated HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
- 9 Aug 2018 Z-3264-2018 Class II Terminated HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
2016
- 5 Jan 2016 Z-1152-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1153-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1154-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1155-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1156-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1157-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1152-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Show the 25 most recent of 33 recalls
2016
- 5 Jan 2016 Z-1158-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1159-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1160-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1161-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1162-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1163-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1164-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1165-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1166-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1167-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1168-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1169-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1170-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1171-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1172-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Full distribution text
- 5 Jan 2016 Z-1158-2017 Class II Terminated Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Sites
- Biomet UK Ltd. GBFEI 3002806535 68 devices
Frequently asked questions
How many devices does Biomet Uk Ltd have in the registry?
The registry currently lists 1354 devices for Biomet Uk Ltd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Uk Ltd's devices?
Among its 50 most recently registered devices, Biomet Uk Ltd has devices listed in EUDAMED (28 devices) and FDA GUDID (22 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Biomet Uk Ltd's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Biomet Uk Ltd's devices are Class I, Class IIa and Class III. Each device page shows its own class and authorisation.
Are there FDA recall records for Biomet Uk Ltd?
FDA recall records list 33 recalls initiated by Biomet Uk Ltd, the most recent initiated on 9 Aug 2018. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Biomet Uk Ltd in the registry?
The most recently registered devices listed for Biomet Uk Ltd include Vanguard™ Complete Knee System, Oxford® Partial Knee System, Vanguard® Knee System and Vanguard® Complete Knee System.