Innotech USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Innotech USA, Inc. makes
Innotech USA, Inc. makes laser devices including the FriendlyLight Nd:YAG lasers, Friendly Light Er:YAG pulsed laser, and LightLance laser skin perforator.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
The Friendlylight Nd: Yag Lasers Ref K033251
Regimes: 510(k) Registry: 510(k)Friendly Light Er:yag Pulsed Laser Ref K000023
Regimes: 510(k) Registry: 510(k)Lightlance Laser Skin Perforator Ref K013021
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innotech USA, Inc. have in the registry?
The registry currently lists 3 devices for Innotech USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innotech USA, Inc.'s devices?
Among its 3 most recently registered devices, Innotech USA, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Innotech USA, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Innotech USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innotech USA, Inc. in the registry?
The most recently registered devices listed for Innotech USA, Inc. include THE FRIENDLYLIGHT ND: YAG LASERS, FRIENDLY LIGHT ER:YAG PULSED LASER and LIGHTLANCE LASER SKIN PERFORATOR.