Medical Device Manufacturer · US , St. Louis , MO

Laser Center Dev. Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Recent clearances: OCULOSTAT, AUTOMATED CORNEAL TREPHINE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Laser Center Dev. Corp. Ophthalmic ✕

2 devices

1-2 of 2

Cleared Jul 15, 1998

Ophthalmic · 103d

Cleared Jun 23, 1998

AUTOMATED CORNEAL TREPHINE

Ophthalmic · 92d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 08, 2026