Kontur Kontact Lens Co., Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2919245
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Kontur 55 Soft Lens Ref K001908
Regimes: 510(k) Registry: 510(k)Kontur 55 Ew Ref P850078
Regimes: PMA Registry: PMA
Company details
- FDA FEI number
- 2919245
- Address
- 642 ALFRED NOBEL DR., Hercules, CA, 94547
Frequently asked questions
How many devices does KONTUR KONTACT LENS CO., INC. have in the registry?
The registry currently lists 2 devices for KONTUR KONTACT LENS CO., INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KONTUR KONTACT LENS CO., INC.'s devices?
Among its 2 most recently registered devices, KONTUR KONTACT LENS CO., INC. has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do KONTUR KONTACT LENS CO., INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for KONTUR KONTACT LENS CO., INC.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from KONTUR KONTACT LENS CO., INC. in the registry?
The most recently registered devices listed for KONTUR KONTACT LENS CO., INC. include KONTUR 55 SOFT LENS and KONTUR 55 EW.