Medical Device Manufacturer · US , Sunnyvale , CA

Visionex, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Visionex, Inc. Ophthalmic ✕

2 devices

1-2 of 2

Cleared Mar 14, 1991

TRABECULO-SUPRACHOROIDAL SHUNT

Ophthalmic · 296d

Cleared May 23, 1988

TEAR VOLUME TESTS

Ophthalmic · 42d

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Apr 28, 2026