Biomet UK Ltd.
Active in EUDAMEDUnited Kingdomfrom SRN EUDAMED FDA SRN GB-MF-000001894 FEI 3002806535
Site of Biomet UK Ltd
Biomet UK Ltd. is a medical device manufacturer based in the United Kingdom, with 68 devices listed in EUDAMED and FDA GUDID (EU Class I, III and IIa) and 33 FDA recalls as of 12 Nov 2026.
- Devices
- 68
- Registrations
- EUDAMEDFDA
- FDA recalls
- 33
Registry facts
- Registries
- EUDAMED 68
- FDA GUDID 29
- Device classes
- EU Class I 33
- EU Class III 20
- EU Class IIa 15
- Top EMDN categories
- FDA recalls
- Sites and related companies
- Identifiers
- EUDAMED SRN GB-MF-000001894
- FDA FEI 3002806535
At a glance
EU certificates
2 of 2 in force.
Market reach
- European Union
- EUDAMED actor, 2 certificates
- United States
- FDA FEI, FDA recalls
Catalogue
Search and filter all 68 devicesShowing 1-50 of 68
Company details
- EUDAMED SRN
- GB-MF-000001894
- FDA FEI number
- 3002806535
- EU VAT number
- GB194814043
- EUDAMED status
- Active
- EUDAMED registered name
- Biomet UK Ltd
- Registered address
- Waterton Industrial Estate, CF31 3XA, Bridgend, United Kingdom (ex Northern Ireland)
- Website
- labeling.zimmerbiomet.com/
- Phone
- +1(800)348-9500
- PRRC contact
- Rhys Holder
EUDAMED certificates
2 certificates2 valid, 0 expiredMDR 2next expiry 6 Nov 2027
BSI Group The Netherlands B.V. 2797 2 certificates
- MDR 754277 Expiring
Technical documentation EU MDR
- Issued
- 11 Aug 2026
- Expires
- 6 Nov 2027
- Reason
- Other
- MDR 754285 Expiring
Technical documentation EU MDR
- Issued
- 9 Sep 2026
- Expires
- 6 Nov 2027
- Reason
- Other
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.
Frequently asked questions
How many devices does BIOMET UK LTD. have in the registry?
The registry currently lists 68 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 (50 devices) and FDA GUDID (14 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 EUDAMED certificates are recorded for BIOMET UK LTD.?
EUDAMED lists 2 certificates for BIOMET UK LTD. (technical documentation) under MDR. The most recent was issued on 9 Sep 2026.
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.