Persol America, Inc.
Country not established
- Devices
- 1
What Persol America, Inc. makes
Persol America, Inc. makes eyewear products including the Persol, Moschino, and Gerald Genta brands.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Persol, Mosclhino, And Gerald Genta Ref K942845
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Persol America, Inc. have in the registry?
The registry currently lists 1 device for Persol America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Persol America, Inc.'s devices?
Among its 1 most recently registered device, Persol America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Persol America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Persol America, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Persol America, Inc. in the registry?
The most recently registered devices listed for Persol America, Inc. include PERSOL, MOSCLHINO, AND GERALD GENTA.