Seiko Optical Products of America, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Seiko Optical Products of America, Inc. makes
Seiko Optical Products of America, Inc. manufactures single-vision AR DIACOAT spectacle lenses, prescription spectacle lenses (Seiko P-2 and P-3), non-prescription sunglasses, and eyeglass frames.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Ar Diacoat Single Vision Lenses Ref K873245
Regimes: 510(k) Registry: 510(k)Seiko P-2 & Seiko P-3 (Spectacle Lens) Ref K861684
Regimes: 510(k) Registry: 510(k)Sunglass, Non-Prescription Ref K900764
Regimes: 510(k) Registry: 510(k)Seiko Eyeglass Frame Ref K942513
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seiko Optical Products of America, Inc. have in the registry?
The registry currently lists 4 devices for Seiko Optical Products of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seiko Optical Products of America, Inc.'s devices?
Among its 4 most recently registered devices, Seiko Optical Products of America, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Seiko Optical Products of America, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Seiko Optical Products of America, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seiko Optical Products of America, Inc. in the registry?
The most recently registered devices listed for Seiko Optical Products of America, Inc. include AR DIACOAT SINGLE VISION LENSES, SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS), SUNGLASS, NON-PRESCRIPTION and SEIKO EYEGLASS FRAME.