FDA applicant

Gatewood and Associates, Ltd.

Tacoma, WA2 decisions1988–19890 recalls

FDA records 2 decisions for Gatewood and Associates, Ltd. (Tacoma, WA) from 1988 to 1989: 2 510(k) clearances. Most are in product codes GEN (Forceps, General & Plastic Surgery) and EKJ (Burnisher, Operative). 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 Gatewood and Associates, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gatewood and Associates, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Gatewood”

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

Gatewood Splints 1

Gatewood and Associates, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Gatewood”