Innomed, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000014761 FEI 1833053
Innomed, Inc. is a medical device manufacturer based in the United States, with 3,278 devices listed and 1 FDA recall as of 14 Nov 2026.
- Devices
- 3,278
- Registrations
- EUDAMEDFDA
- FDA recalls
- 1
Registry facts
- Registries
- FDA GUDID 2,998
- EUDAMED 2,933
- Device classes
- EU Class I 2,909
- FDA Class I 91
- Top EMDN categories
- FDA recalls
- Sites and related companies
- MediMark Europe SARL. authorised representative
- Identifiers
- EUDAMED SRN US-MF-000014761
- FDA FEI 1833053
- DUNS 878427491
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI, FDA recalls
- Authorised rep.
- MediMark Europe SARL.FR
What Innomed, Inc. makes
Innomed, Inc. manufactures reusable orthopaedic surgical instruments, including implant inserters and extractors, hand-held retractors, drill guides, and external distractors. Their portfolio also covers specialized tools like acetabular reamers, leg procedure positioners, and sterilization/disinfection containers designed for surgical environments.
The company’s devices are classified under FDA categories Class I and Class II, with listings in the EU’s eudamed registry and the FDA’s Unique Device Identifier (UDI) database. The company is headquartered in the United States.
Catalogue
Search and filter all 3,278 devicesShowing 1-50 of 3,278
Company details
- EUDAMED SRN
- US-MF-000014761
- FDA FEI number
- 1833053
- DUNS number
- 878427491
- EUDAMED status
- Active
- EUDAMED registered name
- Innomed, Inc.
- Registered address
- 103, Estus Drive, 31404, Savannah, United States
- Website
- www.innomed.net/
- aaron@innomed.net
- Phone
- +1 912 236 0000
- PRRC contact
- Aaron Ingram
FDA recalls
FDA recall records list 1 recall initiated by Innomed, Inc., initiated on 2024-03-07. The reasons filed fall into these groups: other reasons as filed. 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 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 1
- 2025 0
- 2026 0
2024
- 7 Mar 2024 Z-1753-2024 Class II Completed 54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.
Frequently asked questions
How many devices does Innomed, Inc. have in the registry?
The registry currently lists 3278 devices for Innomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innomed, Inc.'s devices?
Among its 50 most recently registered devices, Innomed, Inc. has devices listed in EUDAMED (39 devices) and FDA GUDID (48 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Innomed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Innomed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for Innomed, Inc.?
FDA recall records list 1 recall initiated by Innomed, Inc., the most recent initiated on 7 Mar 2024. 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 Innomed, Inc. in the registry?
The most recently registered devices listed for Innomed, Inc. include Innomed, Inc. 4541-01, Modified Hip Retractor with Waist Pad, Innomed, Inc. 1252-N-R and Innomed, Inc. 1911.