FDA applicant

Midas Rex Pneumatic Tools, Inc.

Fort Worth, TX12 decisions1985–19972 recalls

FDA records 12 decisions for Midas Rex Pneumatic Tools, Inc. (Fort Worth, TX) from 1985 to 1997: 12 510(k) clearances. Most are in product codes GET (Motor, Surgical Instrument, Pneumatic Powered) and HBB (Motor, Drill, Pneumatic). Its devices cite 7 predicates, 7 of them its own earlier devices. 2 recalls are 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 Midas Rex Pneumatic Tools, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midas Rex Pneumatic Tools, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Midas Rex Pneumatic Tools, 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 “Midas”

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

Midas Intl. Development Corp. 1

Midas Rex Pneumatic Tools, 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?

What has been recalled?

Other applicant names beginning “Midas”