FDA applicant

Allergan Medical

Goleta, CA1 decision2011–20112 recalls

FDA records 1 decision for Allergan Medical (Goleta, CA) in 2011: 1 510(k) clearance. All are in product code LCJ (Tissue Expander And Accessories). Its devices cite 1 predicate, 0 of them its own earlier devices. 2 recalls are linked to its devices, 2 Class I.

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

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

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

2in 2019

2011high 2 (2019) · low 0 (2011)2026

Class I Class II/III not classified

FIG. 1 — Allergan Medical by year, 2011–2026Sources: 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 Optical 2 Allergan Pharmaceuticals, Inc. 1

Allergan Medical

Which product codes does it file in?

Whose devices does it build on?

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”