Spectra Therapy LLC
United Statesfrom the FDA registration address FDA establishment FEI 3008539245
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3008539245
- Address
- 3350 Lapeer Rd, Port Huron, MI, 48060
Frequently asked questions
How many devices does SPECTRA THERAPY LLC have in the registry?
The registry currently lists 2 devices for SPECTRA THERAPY LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list SPECTRA THERAPY LLC's devices?
Among its 2 most recently registered devices, SPECTRA THERAPY LLC has devices listed in FDA GUDID (2 devices).
What risk classes do SPECTRA THERAPY LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for SPECTRA THERAPY LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SPECTRA THERAPY LLC in the registry?
The most recently registered devices listed for SPECTRA THERAPY LLC include LaserWrap A-10 and LaserWrap A-100.