Incappe, Inc.
Country not established
- Devices
- 1
What Incappe, Inc. makes
Incappe, Inc. manufactures the HydroBoot, a medical device designed for lower-limb compression therapy and edema management.
The HydroBoot is classified as a Class II device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
Hydroboot Ref K022233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Incappe, Inc. have in the registry?
The registry currently lists 1 device for Incappe, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Incappe, Inc.'s devices?
Among its 1 most recently registered device, Incappe, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Incappe, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Incappe, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Incappe, Inc. in the registry?
The most recently registered devices listed for Incappe, Inc. include HYDROBOOT.