FDA applicant

Allergan Humphrey

San Leandro, CA3 decisions1987–19900 recalls

FDA records 3 decisions for Allergan Humphrey (San Leandro, CA) from 1987 to 1990: 3 510(k) clearances. Most are in product codes HQE (Instrument, Vitreous Aspiration And Cutting…) and IYO (System, Imaging, Pulsed Echo, Ultrasonic). 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 Humphrey’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergan Humphrey since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Allergan Humphrey’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Optical 2 Allergan Medical 1 Allergan Pharmaceuticals, Inc. 1

Allergan Humphrey

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allergan”