FDA applicant

Triad Surgical Technologies, Inc.

Salt Lake City, UT1 decision2000–20000 recalls

FDA records 1 decision for Triad Surgical Technologies, Inc. (Salt Lake City, UT) in 2000: 1 510(k) clearance. All are in product code JOS (Electrode, Electrosurgical). 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 Surgical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Triad Surgical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

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 Division 4 Triad Medical, Inc. 2

Triad Surgical Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Triad”