Medical Device Manufacturer · US , Santa Clara , CA

The Sanborn Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Sanborn Co. Ophthalmic ✕

2 devices

1-2 of 2

Cleared Jul 20, 1990

SURG-K SURGICAL KERATOMETER

Ophthalmic · 108d

Cleared Jun 27, 1990

VKG 1000, VIDEO KERATOGRAPH

Ophthalmic · 86d

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026