FDA applicant

Triad Medical Division

Walker, MI4 decisions1981–19840 recalls

FDA records 4 decisions for Triad Medical Division (Walker, MI) from 1981 to 1984: 4 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and DYB (Introducer, Catheter). 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 Triad Medical Division’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Triad Medical Division since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Triad Medical Division’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 “Triad”

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

Triad Life Sciences, Inc. 4 Triad Medical, Inc. 2 Triad Surgical Technologies, Inc. 1

Triad Medical Division

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Triad”