Otego Optical, Inc.
Country not established
- Devices
- 1
What Otego Optical, Inc. makes
Otego Optical, Inc. manufactures spectacle frames designed for eyewear, including standard and custom-fit options for adults and children.
The company’s products are regulated as Class I medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Spectacle Frames Ref K922001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Otego Optical, Inc. have in the registry?
The registry currently lists 1 device for Otego Optical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Otego Optical, Inc.'s devices?
Among its 1 most recently registered device, Otego Optical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Otego Optical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Otego Optical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Otego Optical, Inc. in the registry?
The most recently registered devices listed for Otego Optical, Inc. include SPECTACLE FRAMES.