World Aesthetix LLC
United Statesfrom the FDA registration address FDA establishment FEI 3025104654
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3025104654
- Address
- 3740 Saint Johns Bluff Rd S Ste 8, Jacksonville, FL, 32224
Frequently asked questions
How many devices does WORLD AESTHETIX LLC have in the registry?
The registry currently lists 2 devices for WORLD AESTHETIX LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list WORLD AESTHETIX LLC's devices?
Among its 2 most recently registered devices, WORLD AESTHETIX LLC has devices listed in FDA GUDID (2 devices).
What risk classes do WORLD AESTHETIX LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for WORLD AESTHETIX LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from WORLD AESTHETIX LLC in the registry?
The most recently registered devices listed for WORLD AESTHETIX LLC include WORLD AESTHETIX BROAD PULSED LIGHT WAX161286 and NuSkin RF Micro WAX231749.