FDA applicant

Stainless Mfg., Inc.

Mchenry, IL19 decisions1980–19840 recalls

FDA records 19 decisions for Stainless Mfg., Inc. (Mchenry, IL) from 1980 to 1984: 19 510(k) clearances. Most are in product codes HTZ (Instrument, Cutting, Orthopedic) and HXP (Instrument, Bending Or Contouring). 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 Stainless Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stainless Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stainless Mfg., 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

Stainless Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?