Transtimulation Research Inc
United Statesfrom the FDA registration address FDA establishment FEI 3036040187
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
TEA Device Ref K230526
Regimes: 510(k) Registry: 510(k)Patch-TEA (Model TRI-21) Ref K243613
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3036040187
- Address
- 898 N Fair Oaks Ave, Unit C, Pasadena, CA, 91103
Frequently asked questions
How many devices does Transtimulation Research Inc have in the registry?
The registry currently lists 3 devices for Transtimulation Research Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transtimulation Research Inc's devices?
Among its 3 most recently registered devices, Transtimulation Research Inc has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Transtimulation Research Inc's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Transtimulation Research Inc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transtimulation Research Inc in the registry?
The most recently registered devices listed for Transtimulation Research Inc include TEA SNM-FDC01, TEA Device and Patch-TEA (Model TRI-21).