Unimedix, Inc.
Country not established
- Devices
- 1
What Unimedix, Inc. makes
Unimedix, Inc. manufactures the Unimedix Holmium Fiber, a device used in laser-based medical procedures, including urological and dermatological applications.
The company’s portfolio is regulated under FDA Class II devices and listed in the 510(k) clearance registry. Unimedix, Inc. is based in the United States.
Catalogue
Unimedix Holmium Fiber Ref K924424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unimedix, Inc. have in the registry?
The registry currently lists 1 device for Unimedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unimedix, Inc.'s devices?
Among its 1 most recently registered device, Unimedix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Unimedix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unimedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Unimedix, Inc. in the registry?
The most recently registered devices listed for Unimedix, Inc. include UNIMEDIX HOLMIUM FIBER.