FDA applicant

Associated Ent., Inc.

Danville, CA4 decisions1989–19930 recalls

FDA records 4 decisions for Associated Ent., Inc. (Danville, CA) from 1989 to 1993: 4 510(k) clearances. Most are in product codes LDQ (Unnamed device) and LYY (Latex Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Associated Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Associated Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Associated”

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

Associated Medical Products Co. 29 Associated Mills, Inc. 14 Associated Medical 3 Associated Electro-Medical Services, Inc. 2 Associated Medical Devices, Inc. 2 Associated Hospital Services, Inc. 1 Associated Electrolysis Group 1 Associated Premium Corp. 1 Associated Medical Representatives 1 Associated Hearing Instruments 1

Associated Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Associated”