Stortford Medical, LLC
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Restep Dvy System, Model Rsp-101 Ref K090308
Regimes: 510(k) Registry: 510(k)MyNeWT Negative Pressure Wound Therapy System Ref K161432
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stortford Medical, LLC have in the registry?
The registry currently lists 2 devices for Stortford Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stortford Medical, LLC's devices?
Among its 2 most recently registered devices, Stortford Medical, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Stortford Medical, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stortford Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stortford Medical, LLC in the registry?
The most recently registered devices listed for Stortford Medical, LLC include RESTEP DVY SYSTEM, MODEL RSP-101 and MyNeWT Negative Pressure Wound Therapy System.