Momo U.S.A., Inc.
Country not established
- Devices
- 1
What Momo U.S.A., Inc. makes
Momo U.S.A., Inc. manufactures the MOMO DESIGN OR MOMO, a device designed for aesthetic or functional facial contouring, including skin tightening and volume enhancement through non-invasive procedures.
The company’s portfolio is regulated under Class I medical devices in the U.S., with the MOMO DESIGN OR MOMO listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Momo Design Or Momo Ref K972416
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Momo U.S.A., Inc. have in the registry?
The registry currently lists 1 device for Momo U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Momo U.S.A., Inc.'s devices?
Among its 1 most recently registered device, Momo U.S.A., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Momo U.S.A., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Momo U.S.A., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Momo U.S.A., Inc. in the registry?
The most recently registered devices listed for Momo U.S.A., Inc. include MOMO DESIGN OR MOMO.