Star Port Inc
United Statesfrom the FDA registration address FDA establishment FEI 3036035308
- 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
- 3036035308
- Address
- 835 JASMINE ST, Denver, CO, 80220
Frequently asked questions
How many devices does STAR PORT INC have in the registry?
The registry currently lists 7 devices for STAR PORT INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list STAR PORT INC's devices?
Among its 7 most recently registered devices, STAR PORT INC has devices listed in FDA GUDID (7 devices).
What risk classes do STAR PORT INC's devices fall under?
Among its 7 most recently registered devices, the classes recorded for STAR PORT INC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from STAR PORT INC in the registry?
The most recently registered devices listed for STAR PORT INC include Kegel SC-03, Kegel HD-05, Kegel SG-03 and Kegel HCD-L-03.