510(k) Report

FDA applicant

Synergistic Medical Technologies, Inc.

Washington, DC1 decision1993–19930 recalls

FDA records 1 decision for Synergistic Medical Technologies, Inc. (Washington, DC) in 1993: 1 510(k) clearance. All are in product code GAB (Needle, Suturing, Disposable). 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 Synergistic Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Synergistic Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • GABNeedle, Suturing, Disposable1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K932591Endo-JudgeSynergistic Medical Technologies, Inc. · 19933cite it

What has FDA decided for it lately?

  • K932591Endo-JudgeSynergistic Medical Technologies, Inc. · 1993

The one decision as Synergistic Medical Technologies, Inc. →