Tempramed
United Statesfrom the FDA registration address FDA establishment FEI 3012381649
- Devices
- 7
- 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
Company details
- FDA FEI number
- 3012381649
- Address
- 19481 SE 14th St, Sammamish, WA, 98075
Frequently asked questions
How many devices does TEMPRAMED have in the registry?
The registry currently lists 7 devices for TEMPRAMED. Devices recorded under merged duplicate company entries are counted once.
Which registries list TEMPRAMED's devices?
Among its 7 most recently registered devices, TEMPRAMED has devices listed in FDA GUDID (7 devices).
What risk classes do TEMPRAMED's devices fall under?
Among its 7 most recently registered devices, the classes recorded for TEMPRAMED's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from TEMPRAMED in the registry?
The most recently registered devices listed for TEMPRAMED include VIVI MED 31002025, VIVI CAP SMART 12002025, VIVI CAP SMART Cover 12102025 and VIVI CAP 11602022.