Medical Device Manufacturer · US , Lake Success , NY

Cannon U.S.A., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cannon U.S.A., Inc. Ophthalmic ✕

1 devices

1-1 of 1

Cleared Sep 02, 1994

AUTO REF-KERATOMETER, RK-3

Ophthalmic · 116d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 28, 2026