Medi USA, LP
United StatesFDA applicant, unverified FDA FEI 1450371
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Medi Butler Ref K051324
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Medi Strumpf Ref K941926
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1450371
- Address
- 6481 Franz Warner Pkwy, WHITSETT, NC, 27377
Frequently asked questions
How many devices does Medi USA, LP have in the registry?
The registry currently lists 4 devices for Medi USA, LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi USA, LP's devices?
Among its 4 most recently registered devices, Medi USA, LP has devices listed in FDA 510(k) (4 devices).
What risk classes do Medi USA, LP's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medi USA, LP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi USA, LP in the registry?
The most recently registered devices listed for Medi USA, LP include MEDI BUTLER, medi pneumatic compression system (pcs)-genius (Model 652), medi pneumatic compression system (pcs) – brio (Model 651) and MEDI STRUMPF.