510(k) Report

FDA applicant

Mada Medical Products, Inc.

Carlstadt, NJ8 decisions1980–20010 recalls

FDA records 8 decisions for Mada Medical Products, Inc. (Carlstadt, NJ) from 1980 to 2001: 8 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and CAF (Nebulizer (Direct Patient Interface)). 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, anesthesiology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mada 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