Etgar Group H.M.Y.A., Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Etgar Group H.M.Y.A., Ltd. makes
Etgar Group H.M.Y.A., Ltd. manufactures the CRYOSHAPE, a cryosurgical device used for controlled tissue ablation through localized freezing. The system is designed for precision treatment in dermatological and cosmetic applications, targeting benign skin lesions and other targeted tissue modifications.
The CRYOSHAPE is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cryoshape Ref K060928
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Etgar Group H.M.Y.A., Ltd. have in the registry?
The registry currently lists 1 device for Etgar Group H.M.Y.A., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Etgar Group H.M.Y.A., Ltd.'s devices?
Among its 1 most recently registered device, Etgar Group H.M.Y.A., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Etgar Group H.M.Y.A., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Etgar Group H.M.Y.A., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Etgar Group H.M.Y.A., Ltd. in the registry?
The most recently registered devices listed for Etgar Group H.M.Y.A., Ltd. include CRYOSHAPE.