FDA applicant

Allergan Optical

Irvine, CA2 decisions1988–19880 recalls

FDA records 2 decisions for Allergan Optical (Irvine, CA) in 1988: 2 510(k) clearances. Most are in product codes LRX (Case, Contact Lens) and LPN (Accessories, Soft Lens Products). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Allergan Optical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergan Optical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Allergan Optical by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Allergan”

FDA records each applicant name separately; these may or may not be the same firm.

Allergan, Inc. 47 Allergan Medical Optics 7 Allergan Humphrey 3 Allergan Medical 1 Allergan Pharmaceuticals, Inc. 1

Allergan Optical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allergan”