Tecomet, Inc
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000027544 FEI 3003018882
Tecomet, Inc is a medical device manufacturer based in the United States, with 2,336 devices listed in FDA GUDID and EUDAMED (FDA Class I and II; EU Class I) as of 12 Nov 2026.
- Devices
- 2,336
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 2,336
- EUDAMED 288
- Device classes
- FDA Class I 1,914
- EU Class I 263
- FDA Class II 159
- Top EMDN categories
- Sites and related companies
- Meditec Source GmbH & Co. KG authorised representative
- Identifiers
- EUDAMED SRN US-MF-000027544
- FDA FEI 3003018882
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- Meditec Source GmbH & Co. KGDE
What Tecomet, Inc makes
Tecomet, Inc. manufactures reusable surgical instruments, including non-torque-limiting and torque-limiting surgical instrument handles, reusable surgical screwdrivers, and reusable bone curettes. The company also produces orthopaedic implantable-device cutters, bone holding forceps, and reusable hand-held surgical retractors. Specialized devices include the Pistol Guidewire Gripper and sterilization/disinfection containers for surgical tools.
The company’s products are classified under FDA Device Classes I and II and are listed in the FDA’s Unique Device Identifier (UDI) database. Tecomet, Inc. is based in the United States.
Catalogue
Search and filter all 2,336 devicesShowing 1-50 of 2,336
Company details
- EUDAMED SRN
- US-MF-000027544
- FDA FEI number
- 3003018882
- EUDAMED status
- Active
- EUDAMED registered name
- Tecomet,Inc
- EUDAMED abbreviated name
- Tecomet Kenosha
- Registered address
- 5307, 95th Avenue, 53144, Kenosha, United States
- PRRC contact
- Julie Davis
Frequently asked questions
How many devices does Tecomet,Inc have in the registry?
The registry currently lists 2336 devices for Tecomet,Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tecomet,Inc's devices?
Among its 50 most recently registered devices, Tecomet,Inc has devices listed in FDA GUDID (50 devices).
What risk classes do Tecomet,Inc's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Tecomet,Inc's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tecomet,Inc in the registry?
The most recently registered devices listed for Tecomet,Inc include Tecomet 939999518, Tecomet MA101000-J, Tecomet S-201080 and Tecomet MSI-10001.