Medical Device Manufacturer · US , Winter Park , FL

Lasersight Technologies, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1998

Recent clearances: ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS, ULTRASHAPER KERATOME, AUTOMATED DISPOSABLE KERATOME (ADK)

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

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

3 devices

1-3 of 3

Cleared May 05, 2000

ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS

Ophthalmic · 25d

Cleared Jan 31, 2000

ULTRASHAPER KERATOME

Ophthalmic · 371d

Cleared Jan 08, 1998

AUTOMATED DISPOSABLE KERATOME (ADK)

Ophthalmic · 79d