510(k) Report

FDA applicant

Tecnol Medical Products, Inc.

Fort Worth, TX21 decisions1992–19971 recall

FDA records 21 decisions for Tecnol Medical Products, Inc. (Fort Worth, TX) from 1992 to 1997: 21 510(k) clearances. Most are in product codes FMQ (Restraint, Protective) and FXX (Mask, Surgical). 1 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 hospital panel, where it files most

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

FDA decisions per year

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

Recalls per year

1in 2023

2023: 1
2007high 1 (2023) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Tecnol Medical Products, 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 “Tecnol”

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