Rodenstock USA Inc.,
Country not established
- Devices
- 1
What Rodenstock USA Inc., makes
Rodenstock USA Inc. manufactures spectacle frames, which are designed for corrective and protective eyewear. These products are intended for general use in optical prescriptions and include a range of styles for adults and children.
The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These products are intended for use within the United States.
Catalogue
Spectacle Frames Ref K943039
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rodenstock USA Inc., have in the registry?
The registry currently lists 1 device for Rodenstock USA Inc.,. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rodenstock USA Inc.,'s devices?
Among its 1 most recently registered device, Rodenstock USA Inc., has devices listed in FDA 510(k) (1 device).
What risk classes do Rodenstock USA Inc.,'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rodenstock USA Inc.,'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rodenstock USA Inc., in the registry?
The most recently registered devices listed for Rodenstock USA Inc., include SPECTACLE FRAMES.