FDA applicant

Temp Medical Products, Inc.

Mchenry, IL2 decisions1980–19830 recalls

FDA records 2 decisions for Temp Medical Products, Inc. (Mchenry, IL) from 1980 to 1983: 2 510(k) clearances. Most are in product codes DWH (Blade, Saw, Surgical, Cardiovascular) and DWI (Saw, Electrically Powered). 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 Temp Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Temp Medical Products, 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 “Temp”

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

Temp-Stik Corp. 3

Temp Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Temp”