MD Labs, LLC
United Statesfrom the FDA registration address FDA FEI 3027686087
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
HydraDose Vaginal Suppositories Ref K230518
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3027686087
- DUNS number
- 123340634
- Address
- 780 Lakefield Rd., Westlake Village, CA, 91361
Frequently asked questions
How many devices does MD Labs, LLC have in the registry?
The registry currently lists 2 devices for MD Labs, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MD Labs, LLC's devices?
Among its 2 most recently registered devices, MD Labs, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MD Labs, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for MD Labs, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MD Labs, LLC in the registry?
The most recently registered devices listed for MD Labs, LLC include HYDRADOSE MD_01 and HydraDose Vaginal Suppositories.