Discovery Group, LLC
Country not established
- Devices
- 1
What Discovery Group, LLC makes
Discovery Group, LLC manufactures the FLO-BOOT, a device designed for foot hygiene and circulation support, typically used in clinical or post-operative care settings.
The FLO-BOOT is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Flo-Boot Ref K003272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Discovery Group, LLC have in the registry?
The registry currently lists 1 device for Discovery Group, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Discovery Group, LLC's devices?
Among its 1 most recently registered device, Discovery Group, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Discovery Group, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Discovery Group, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Discovery Group, LLC in the registry?
The most recently registered devices listed for Discovery Group, LLC include FLO-BOOT.