Kryoderm USA, Inc.
Country not established
- Devices
- 1
What Kryoderm USA, Inc. makes
Kryoderm USA, Inc. manufactures the ERGOMED, a cryotherapy device designed for controlled application of cold therapy to treat skin conditions.
The company’s portfolio is regulated under FDA Class II devices, with the ERGOMED authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Ergomed Ref K912529
510(k) 510(k)
Frequently asked questions
How many devices does Kryoderm USA, Inc. have in the registry?
The registry currently lists 1 device for Kryoderm USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kryoderm USA, Inc.'s devices?
Among its 1 most recently registered device, Kryoderm USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kryoderm USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kryoderm USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kryoderm USA, Inc. in the registry?
The most recently registered devices listed for Kryoderm USA, Inc. include ERGOMED.