Jereva, Inc.
Country not established
- Devices
- 1
What Jereva, Inc. makes
Jereva, Inc. manufactures the LEG EEZE, a device designed for lower extremity edema management, likely incorporating compression or lymphatic drainage technology.
The LEG EEZE 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
Leg Eeze Ref K901931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jereva, Inc. have in the registry?
The registry currently lists 1 device for Jereva, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jereva, Inc.'s devices?
Among its 1 most recently registered device, Jereva, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jereva, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jereva, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jereva, Inc. in the registry?
The most recently registered devices listed for Jereva, Inc. include LEG EEZE.