Wellquest Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Wellquest Intl., Inc. makes
Wellquest Intl., Inc. manufactures hair removal devices, including the Nubrillance pulsed light system and the Dapelle hair remover, designed for at-home use.
These devices are regulated under FDA Class I and Class II classifications, with relevant products listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Nubrilliance Pulsed Light Hair Removal Device Ref K132518
Regimes: 510(k) Registry: 510(k)Dapelle Hair Remover Ref K973773
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wellquest Intl., Inc. have in the registry?
The registry currently lists 2 devices for Wellquest Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wellquest Intl., Inc.'s devices?
Among its 2 most recently registered devices, Wellquest Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Wellquest Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wellquest Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wellquest Intl., Inc. in the registry?
The most recently registered devices listed for Wellquest Intl., Inc. include NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE and DAPELLE HAIR REMOVER.