FDA applicant

Trident Medical Products, Inc.

Fort Worth, TX3 decisions1989–19890 recalls

FDA records 3 decisions for Trident Medical Products, Inc. (Fort Worth, TX) in 1989: 3 510(k) clearances. Most are in product codes HOY (Shield, Eye, Ophthalmic (Including Sunlamp…) and KKX (Drape, Surgical, Antimicrobial). 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, ophthalmic panel, where it files most

How often FDA has decided Trident Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trident Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Trident Medical Products, 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 “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 Surgical Corp. 2 Trident Orthopedics 1

Trident Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Trident”