Footdocprenur, LLC
Country not established
- Devices
- 1
What Footdocprenur, LLC makes
Footdocprenur, LLC manufactures the REMY Medical Therapy Laser System, a Class II device designed for therapeutic laser treatments.
The REMY Medical Therapy Laser System is regulated under FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
REMY Medical Therapy Laser System Ref K190034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Footdocprenur, LLC have in the registry?
The registry currently lists 1 device for Footdocprenur, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Footdocprenur, LLC's devices?
Among its 1 most recently registered device, Footdocprenur, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Footdocprenur, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Footdocprenur, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Footdocprenur, LLC in the registry?
The most recently registered devices listed for Footdocprenur, LLC include REMY Medical Therapy Laser System.