510(k) Report

FDA applicant

Safe Tech Medical Products, Inc.

Houston, TX2 decisions1990–19910 recalls

FDA records 2 decisions for Safe Tech Medical Products, Inc. (Houston, TX) from 1990 to 1991: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Safe Tech Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Safe Tech 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 “Safe”

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