Sunetics International Marketing Group, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Sunetics International Marketing Group, LLC makes
Sunetics International Marketing Group, LLC manufactures the SUNETICS Clinical Bio-Stimulation Laser, a medical laser device designed for therapeutic applications, and the LASERBRUSH, a laser-assisted cleaning tool for medical instruments.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sunetics Clinical Bio-Stimulation Laser Ref K132646
Regimes: 510(k) Registry: 510(k)Laserbrush Ref K121920
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sunetics International Marketing Group, LLC have in the registry?
The registry currently lists 2 devices for Sunetics International Marketing Group, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sunetics International Marketing Group, LLC's devices?
Among its 2 most recently registered devices, Sunetics International Marketing Group, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Sunetics International Marketing Group, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sunetics International Marketing Group, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sunetics International Marketing Group, LLC in the registry?
The most recently registered devices listed for Sunetics International Marketing Group, LLC include SUNETICS CLINICAL BIO-STIMULATION LASER and LASERBRUSH.