FDA applicant

Trinity Laboratories, Inc.

Salisbury, MD44 decisions1990–19980 recalls

FDA records 44 decisions for Trinity Laboratories, Inc. (Salisbury, MD) from 1990 to 1998: 44 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and MCZ (Suture Removal Kit). 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 Trinity Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trinity Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Trinity”

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

Trinity Biotech, Plc 12 Trinity Biotech USA 11 Trinity Orthopedics, LLC 2 Trinity Partners, LLC 1 Trinity Medical Solutions 1 Trinity Biotech (Primus Corporation, Dba Trinity… 1 Trinity Guardion 1

Trinity Laboratories, Inc.

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 “Trinity”