510(k) Report

FDA applicant

Medtrax Industries, Inc.

Longwood, FL6 decisions1993–19940 recalls

FDA records 6 decisions for Medtrax Industries, Inc. (Longwood, FL) from 1993 to 1994: 6 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Medtrax Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtrax Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medtrax Industries, Inc.’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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