Conmed Corporation
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000012663 FEI 3001451571
Conmed Corporation is a medical device manufacturer based in the United States, with 5,775 devices listed and 178 FDA recalls as of 12 Nov 2026.
- Devices
- 5,775
- Registrations
- EUDAMEDFDA
- FDA recalls
- 17812 ongoing
Registry facts
- Registries
- FDA GUDID 3,000
- EUDAMED 2,105
- FDA 510(k) 7
- FDA PMA 1
- Device classes
- FDA Class II 1,038
- EU Class IIa 651
- FDA Class I 648
- EU Class I 418
- EU Class IIb 194
- FDA Class III 26
- Top EMDN categories
- Arthroscopy devices, single-use 353
- Orthopaedic prostheses, osteosynthesis devices, devices for tendon and ligament synthesis 197
- Instruments for functional explorations and therapeutic interventions 176
- Orthopaedic and traumatological surgery instruments, reusable 152
- Electrosurgery devices, single-use 61
- Arrhythmology devices 54
- FDA recalls
- Sites and related companies
- Conmed Europe BV authorised representative
- MDSS GmbH authorised representative
- Identifiers
- EUDAMED SRN US-MF-000012663
- FDA FEI 3001451571
- DUNS 071595540
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI, FDA recalls
- Authorised rep.
- Conmed Europe BVBE
- Authorised rep.
- MDSS GmbHDE
What Conmed Corporation makes
Conmed Corporation manufactures single-use orthopaedic burs, oscillating surgical saw blades, and monopolar electrosurgical electrodes for open surgery. Their reusable products include electrical connection cables, tendon/ligament bone anchors, electrocardiographic lead sets, and scissors-like soft-tissue manipulation forceps. The company also produces bioabsorbable orthopaedic bone screws and non-bioabsorbable tendon/ligament anchors.
The portfolio includes devices classified under FDA categories Class I, II, III, and Unclassified (U), all listed in the FDA’s Unique Device Identification (UDI) database. The company is based in the United States.
Catalogue
Search and filter all 5,775 devicesShowing 1-50 of 5,775
Company details
- EUDAMED SRN
- US-MF-000012663
- FDA FEI number
- 3001451571
- DUNS number
- 071595540
- EU VAT number
- BE0463870133
- EUDAMED status
- Active
- EUDAMED registered name
- Conmed Corporation
- Registered address
- 525, French Road, 13502, Utica, United States
- Website
- www.conmed.com/
- Phone
- +1 866-426-6633
- PRRC contact
- Brent Lalomia
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 18 May 2027
BSI Group The Netherlands B.V. 2797 1 certificate
- MDR 736992 Expiring
Quality management system EU MDR
- Issued
- 22 Jul 2026
- Expires
- 18 May 2027
- Reason
- Add device or group
FDA recalls
FDA recall records list 178 recalls initiated by Conmed Corporation, the earliest on 2003-07-30 and the most recent on 2026-07-14. By recorded status: 12 ongoing and 166 terminated. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination, packaging, mechanical integrity, performance or accuracy and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 8
- 2018 5
- 2019 6
- 2020 2
- 2021 2
- 2022 1
- 2023 0
- 2024 0
- 2025 0
- 2026 12
2026
- 14 Jul 2026 Z-3018-2026 Class II Ongoing Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- 14 May 2026 Z-2464-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2465-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2466-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2467-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2468-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2469-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2470-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2471-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2472-2026 Class II Ongoing Potential for overpressure alerts.
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Show the 25 most recent of 178 recalls
2026
- 14 May 2026 Z-2473-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2474-2026 Class II Ongoing Potential for overpressure alerts.
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- 14 May 2026 Z-2473-2026 Class II Ongoing Potential for overpressure alerts.
2022
- 18 Nov 2022 Z-0474-2023 Class II Terminated Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
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- 18 Nov 2022 Z-0474-2023 Class II Terminated Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
2021
- 26 Mar 2021 Z-1498-2021 Class II Terminated Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used
- 26 Mar 2021 Z-1499-2021 Class II Terminated Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used
2020
- 12 Nov 2020 Z-0650-2021 Class II Terminated Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
- 12 Nov 2020 Z-0651-2021 Class II Terminated Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
2019
- 21 Mar 2019 Z-1304-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1305-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1306-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1307-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1308-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1309-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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- 21 Mar 2019 Z-1304-2019 Class II Terminated Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
2018
- 23 Feb 2018 Z-1174-2018 Class II Terminated Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
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- 23 Feb 2018 Z-1175-2018 Class II Terminated Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
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- 23 Feb 2018 Z-1174-2018 Class II Terminated Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
Frequently asked questions
How many devices does Conmed Corporation have in the registry?
The registry currently lists 5775 devices for Conmed Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Conmed Corporation's devices?
Among its 50 most recently registered devices, Conmed Corporation has devices listed in EUDAMED (6 devices) and FDA GUDID (47 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Conmed Corporation's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Conmed Corporation's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Conmed Corporation?
FDA recall records list 178 recalls initiated by Conmed Corporation, the most recent initiated on 14 Jul 2026. 12 of them are recorded as ongoing. 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 Conmed Corporation?
EUDAMED lists 1 certificate for Conmed Corporation (quality management system) under MDR. The most recent was issued on 22 Jul 2026.
What are the newest devices from Conmed Corporation in the registry?
The most recently registered devices listed for Conmed Corporation include MicroFree®, Argo Knotless KBC475-KIT, Argo Knotless K475-KIT and CORE DYNAMICS CD1406.