USA Laser Therapeutics, Inc.
Country not established
- Devices
- 1
What USA Laser Therapeutics, Inc. makes
Usa Laser Therapeutics, Inc. manufactures the BODIHEALTH SYSTEM, a Class II medical device designed for laser-based therapeutic applications, likely targeting soft tissue or musculoskeletal conditions through controlled energy delivery.
The BODIHEALTH SYSTEM is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Bodihealth System Ref K052836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Usa Laser Therapeutics, Inc. have in the registry?
The registry currently lists 1 device for Usa Laser Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usa Laser Therapeutics, Inc.'s devices?
Among its 1 most recently registered device, Usa Laser Therapeutics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Usa Laser Therapeutics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Usa Laser Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usa Laser Therapeutics, Inc. in the registry?
The most recently registered devices listed for Usa Laser Therapeutics, Inc. include BODIHEALTH SYSTEM.