Gti, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Gti, Inc. makes
Gti, Inc. manufactures sunlamp models 24N, 30R, 30RE, and 37RE, as well as the GTI clasp cover.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Sunlamp Models 24N, 30R, 30RE, 37RE Ref K860347
Regimes: 510(k) Registry: 510(k)Gti Clasp Cover Ref K913200
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gti, Inc. have in the registry?
The registry currently lists 2 devices for Gti, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gti, Inc.'s devices?
Among its 2 most recently registered devices, Gti, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gti, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gti, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gti, Inc. in the registry?
The most recently registered devices listed for Gti, Inc. include SUNLAMP MODELS 24N, 30R, 30RE, 37RE and GTI CLASP COVER.