Kopharm, Inc.
Country not established
- Devices
- 1
What Kopharm, Inc. makes
Kopharm, Inc. manufactures micro-thin contact lenses, including the UTAGE-MATSU and UTAGE-SAKURA designs, intended for corneal reshaping therapy.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Utage-Matsu-Micro-Thin Utage-Sakura, Ref K800518
510(k) 510(k)
Frequently asked questions
How many devices does Kopharm, Inc. have in the registry?
The registry currently lists 1 device for Kopharm, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kopharm, Inc.'s devices?
Among its 1 most recently registered device, Kopharm, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kopharm, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kopharm, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kopharm, Inc. in the registry?
The most recently registered devices listed for Kopharm, Inc. include UTAGE-MATSU-MICRO-THIN UTAGE-SAKURA,.