Midwest Eye Laboratories, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000116180
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Artificial Scleral Shell Ref K904961
Regimes: 510(k) Registry: 510(k)Eye Artificial Custom Ref K904962
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000116180
- Address
- 20 2ND AVE., S.W., ROCHESTER, MN, 55901
Frequently asked questions
How many devices does MIDWEST EYE LABORATORIES, INC. have in the registry?
The registry currently lists 5 devices for MIDWEST EYE LABORATORIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MIDWEST EYE LABORATORIES, INC.'s devices?
Among its 5 most recently registered devices, MIDWEST EYE LABORATORIES, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MIDWEST EYE LABORATORIES, INC.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for MIDWEST EYE LABORATORIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MIDWEST EYE LABORATORIES, INC. in the registry?
The most recently registered devices listed for MIDWEST EYE LABORATORIES, INC. include Eye, Artificial, Non-Custom V2623, Shell, Scleral V2627, Ophthalmic Conformer V2628 and ARTIFICIAL SCLERAL SHELL.