FDA applicant

Trident Surgical Corp.

Mchenry, IL2 decisions1981–19820 recalls

FDA records 2 decisions for Trident Surgical Corp. (Mchenry, IL) from 1981 to 1982: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HAM (Apparatus, 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 Trident Surgical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trident Surgical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Trident Surgical Corp.’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 “Trident”

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

Trident S.R.L 5 Trident Dental, Inc. 3 Trident Medical Products, Inc. 3 Trident Orthopedics 1

Trident Surgical Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Trident”