Medical Device Manufacturer · US , Irvine , CA

Allergan Optical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Allergan Optical Ophthalmic ✕

2 devices

1-2 of 2

Cleared Dec 28, 1988

ALLERGAN LENS CASE

Ophthalmic · 78d

Cleared Jun 09, 1988

DURACLEAN DAILY CLEANER

Ophthalmic · 29d

Data Source

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

Last updated: Apr 28, 2026