510(k) Report

FDA applicant

Midland Mfg. Co.

Great Neck, NY7 decisions1992–19940 recalls

FDA records 7 decisions for Midland Mfg. Co. (Great Neck, NY) from 1992 to 1994: 7 510(k) clearances. Most are in product codes INQ (Table, Powered) and BXB (Exerciser, 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, physical medicine panel, where it files most

How often FDA has decided Midland Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midland Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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