CC Wellness LLC
United StatesFDA applicant, unverified FDA FEI 3013395518
CC Wellness LLC is a medical device manufacturer, with 683 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 683
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 671
- FDA 510(k) 12
- Device classes
- FDA Class II 683
- Identifiers
- FDA FEI 3013395518
- DUNS 067692292
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 683 devicesShowing 1-50 of 683
Company details
- FDA FEI number
- 3013395518
- DUNS number
- 067692292
- Address
- 24903 Avenue Kearny, Valencia, CA, 91355
Frequently asked questions
How many devices does CC Wellness LLC have in the registry?
The registry currently lists 683 devices for CC Wellness LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list CC Wellness LLC's devices?
Among its 50 most recently registered devices, CC Wellness LLC has devices listed in FDA GUDID (50 devices).
What risk classes do CC Wellness LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for CC Wellness LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CC Wellness LLC in the registry?
The most recently registered devices listed for CC Wellness LLC include Beacon Wellness Fertility Friendly Lubricant - Ecommerce 72315-EC, LL 3x Anal 5mL Foils - 10pk 75026, LL Silky Silicone 5mL Foils - 10pk 75027 and Beacon Wellness - Menopause Lubricant - 2oz / 60mL 72317.