Kt Optique, Inc.
JapanFDA 510(k) applicant, unverified
- Devices
- 1
What Kt Optique, Inc. makes
Kt Optique, Inc. manufactures spectacle frames designed for corrective and fashion eyewear. These frames are intended for general use in optical prescriptions and may include features for comfort, durability, and aesthetic appeal.
The company’s spectacle frames are classified as Class I medical devices under FDA regulations, with records supported by 510(k) submissions. The products are listed in the FDA’s 510(k) database and comply with U.S. device standards.
Catalogue
Spectacle Frames Ref K943792
510(k) 510(k)
Frequently asked questions
How many devices does Kt Optique, Inc. have in the registry?
The registry currently lists 1 device for Kt Optique, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kt Optique, Inc.'s devices?
Among its 1 most recently registered device, Kt Optique, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kt Optique, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kt Optique, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kt Optique, Inc. in the registry?
The most recently registered devices listed for Kt Optique, Inc. include SPECTACLE FRAMES.