Microvision, Inc.

United StatesFDA 510(k) applicant, unverified FDA FEI 3002532015

Devices: 62
Registrations: FDA
FDA recalls: 0

Catalogue62

Newest first, page 2 of 2

N/A 5152

Class I FDA UDI Active
N/A 5162

Class I FDA UDI Active
N/A 5147

Class I FDA UDI Active
NA Style 279 Ref Style 279

Class II FDA UDI Active
Na 5124

Class II FDA UDI Active
N/A 5016-5

Class I FDA UDI Active
NA Style 112 Ref Style 112

Class II FDA UDI Active
NA Style 506 Ref Style 506

Class II FDA UDI Active
N/A 5188

Class I FDA UDI Active
Fiber Optic Endoillumination Probe Ref K982462

Class II FDA 510(k) Active
Microvision Scleral Buckling Components Ref K023481

Class II FDA 510(k) Active
Scleral Plugs, 19 And 20 Gauge Ref K022186

Class II FDA 510(k) Active

Showing 51-62 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.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.