Joylux, Inc.
Country not established FDA FEI 3012262584
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
Joylux Intimacy Gel (PG3100) Ref K242958
510(k) 510(k)
Company details
- FDA FEI number
- 3012262584
- DUNS number
- 079956040
- Address
- 5628 Airport Way S Ste 210, Seattle, WA, 98108
- [email protected]
- Phone
- 844-872-8578
Frequently asked questions
How many devices does Joylux, Inc. have in the registry?
The registry currently lists 6 devices for Joylux, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Joylux, Inc.'s devices?
Among its 6 most recently registered devices, Joylux, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Joylux, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Joylux, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Joylux, Inc. in the registry?
The most recently registered devices listed for Joylux, Inc. include JUICY LIKE A PEACH JLD124, ILYEO body JLD113, Joylux JLD109 and Joylux JLD107.