Global USA Distribution, LLC
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Skinclear Q-Switched Nd:yag Laser Ref K083272
Regimes: 510(k) Registry: 510(k)Skin Clear Srvh Long-Pulsed Nd: Yag Laser Ref K080697
Regimes: 510(k) Registry: 510(k)Nannolight Intense Pulsed Light System Ref K082033
Regimes: 510(k) Registry: 510(k)Laserpeel Soft-Met Modified Erbium Laser Ref K082028
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Global USA Distribution, LLC have in the registry?
The registry currently lists 4 devices for Global USA Distribution, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Global USA Distribution, LLC's devices?
Among its 4 most recently registered devices, Global USA Distribution, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Global USA Distribution, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Global USA Distribution, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Global USA Distribution, LLC in the registry?
The most recently registered devices listed for Global USA Distribution, LLC include SKINCLEAR Q-SWITCHED ND:YAG LASER, SKIN CLEAR SRVH LONG-PULSED ND: YAG LASER, NANNOLIGHT INTENSE PULSED LIGHT SYSTEM and LASERPEEL SOFT-MET MODIFIED ERBIUM LASER.