FDA applicant

Allergan Medical Optics

Anasco, PR7 decisions1989–19952 recalls

FDA records 7 decisions for Allergan Medical Optics (Anasco, PR) from 1989 to 1995: 7 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and KYB (Lens, Guide, Intraocular). 2 recalls are 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 Medical Optics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergan Medical Optics since 2007.

Recalls per year

1in 2022

2007high 1 (2022) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Allergan Medical Optics 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 Humphrey 3 Allergan Optical 2 Allergan Medical 1 Allergan Pharmaceuticals, Inc. 1

Allergan Medical Optics

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Allergan”