Surgilight, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Surgilight, Inc Excimer Laser Ref K993328
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgilight, Inc. have in the registry?
The registry currently lists 2 devices for Surgilight, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgilight, Inc.'s devices?
Among its 2 most recently registered devices, Surgilight, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Surgilight, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Surgilight, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgilight, Inc. in the registry?
The most recently registered devices listed for Surgilight, Inc. include EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO and SURGILIGHT, INC EXCIMER LASER.