Trumedx LLC
United Statesfrom the FDA registration address FDA establishment FEI 3032062344
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3032062344
- Address
- 1 Parrott Dr Ste 400, Shelton, CT, 06484
Frequently asked questions
How many devices does TRUMEDX LLC have in the registry?
The registry currently lists 10 devices for TRUMEDX LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list TRUMEDX LLC's devices?
Among its 10 most recently registered devices, TRUMEDX LLC has devices listed in FDA GUDID (10 devices).
What risk classes do TRUMEDX LLC's devices fall under?
Among its 10 most recently registered devices, the classes recorded for TRUMEDX LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from TRUMEDX LLC in the registry?
The most recently registered devices listed for TRUMEDX LLC include TruEMS TRU-X101, TruDVT TRU-X100, Mobil-IZE KNEE TRU-X103 and Bighorn Ice Plus Compression TRU-X102.