Retropsoas Technologies, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3031284747
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
EARP Nerve Cuff Electrode Ref K241917
Regimes: 510(k) Registry: 510(k)EARP Interbody System Ref K242457
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3031284747
- Address
- 34 Countryside Lane, Frontenac, MO, 63131
Frequently asked questions
How many devices does RETROPSOAS TECHNOLOGIES, LLC have in the registry?
The registry currently lists 2 devices for RETROPSOAS TECHNOLOGIES, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list RETROPSOAS TECHNOLOGIES, LLC's devices?
Among its 2 most recently registered devices, RETROPSOAS TECHNOLOGIES, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do RETROPSOAS TECHNOLOGIES, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for RETROPSOAS TECHNOLOGIES, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from RETROPSOAS TECHNOLOGIES, LLC in the registry?
The most recently registered devices listed for RETROPSOAS TECHNOLOGIES, LLC include EARP Nerve Cuff Electrode and EARP Interbody System.