Microvision, Inc.
United StatesFDA 510(k) applicant, unverified FDA FEI 3002532015
- Devices
- 62
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
NA Style 70 Ref Style 70
NA Style 286 Ref Style 286
NA Style 48 Ref Style 48
NA Style 270 Ref Style 270
NA Style 503 Ref Style 503
NA Style 287 Ref Style 287
NA Style 42 Ref Style 42
NA Style 507 Ref Style 507
NA Style 277 Ref Style 277
NA Style 240 Ref Style 240
NA Style 504 Ref Style 504
NA Style 40 Ref Style 40
NA Style 106 Ref Style 106
NA Style 505 Ref Style 505
NA Style 276 Ref Style 276
Showing 1-50 of 62
Company details
- FDA FEI number
- 3002532015
- DUNS number
- 013486803
- Address
- 20 London Ln, SEABROOK, NH, 03874
What Microvision, Inc. makes
Microvision, Inc. makes fiber optic endoillumination probes, scleral buckling components, and scleral plugs in 19 and 20 gauge sizes.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Frequently asked questions
How many devices does MICROVISION, INC. have in the registry?
The registry currently lists 62 devices for MICROVISION, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MICROVISION, INC.'s devices?
Among its 50 most recently registered devices, MICROVISION, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do MICROVISION, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for MICROVISION, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MICROVISION, INC. in the registry?
The most recently registered devices listed for MICROVISION, INC. include NA Style 70, NA 5177, NA 5038 and NA 5126.