Medic Sharplight, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Medic Sharplight, Ltd. makes
Medic Sharplight, Ltd. manufactures the BEAMAX, a medical device designed for precise light-based procedures, likely in surgical or dermatological applications.
The BEAMAX is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Beamax Ref K063249
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medic Sharplight, Ltd. have in the registry?
The registry currently lists 1 device for Medic Sharplight, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medic Sharplight, Ltd.'s devices?
Among its 1 most recently registered device, Medic Sharplight, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medic Sharplight, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medic Sharplight, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medic Sharplight, Ltd. in the registry?
The most recently registered devices listed for Medic Sharplight, Ltd. include BEAMAX.