Seiko Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Seiko Corp. makes
Seiko Corp. manufactures spectacle frames and progressive spectacle lenses designed for vision correction, including the Seiko P-6 Progressive lenses.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Spectacle Frame Ref K900732
Regimes: 510(k) Registry: 510(k)Seiko P-6 Progressive Spectacle Lenses Ref K884360
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seiko Corp. have in the registry?
The registry currently lists 2 devices for Seiko Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seiko Corp.'s devices?
Among its 2 most recently registered devices, Seiko Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Seiko Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Seiko Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seiko Corp. in the registry?
The most recently registered devices listed for Seiko Corp. include SPECTACLE FRAME and SEIKO P-6 PROGRESSIVE SPECTACLE LENSES.