Medical Device Manufacturer · US , Santa Clara , CA

Kera Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kera Corp. Ophthalmic ✕

4 devices

1-4 of 4

Cleared May 30, 1990

MODEL 2000 INTRAOPERATIVE CORNEASCOPE

Ophthalmic · 86d

Cleared May 22, 1987

Ophthalmic · 38d

Cleared Nov 13, 1986

KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER

Ophthalmic · 28d

Cleared Mar 20, 1985

CORNEASCOPE MODEL 1200

Ophthalmic · 28d

Data Source

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

Last updated: Apr 27, 2026