FDA applicant

Acumed Instruments Corp.

Santa Barbara, CA8 decisions1979–19860 recalls

FDA records 8 decisions for Acumed Instruments Corp. (Santa Barbara, CA) from 1979 to 1986: 8 510(k) clearances. Most are in product codes GFF (Bur, Surgical, General & Plastic Surgery) and CAC (Apparatus, Autotransfusion). 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 and plastic surgery panel, where it files most

How often FDA has decided Acumed Instruments Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Acumed Instruments Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Acumed”

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

Acumed, LLC 38 Acumed Technologies, Inc. 1 Acumed Medical Supplies, Ltd. 1 Acumed Medical, Ltd. 1

Acumed Instruments Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Acumed”