Genemed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Genemed, Inc. makes
Genemed, Inc. manufactures the GeneMed YAG 1000 Medical Laser, a device designed for medical laser applications, and the Genestone Exel (XL) Extracorporeal Shock Wave Lithotripter, used for breaking up kidney stones through shockwave therapy.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Genemed Yag 1000 Medical Laser Ref K943479
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genemed, Inc. have in the registry?
The registry currently lists 2 devices for Genemed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genemed, Inc.'s devices?
Among its 2 most recently registered devices, Genemed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Genemed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Genemed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genemed, Inc. in the registry?
The most recently registered devices listed for Genemed, Inc. include GENEMED YAG 1000 MEDICAL LASER and GENESTONE EXEL (XL) EXTRACORPOREAL SHOCK WAVE LITHOTRIPTER.