510(k) Report

FDA applicant

Medical Equipment Development Co., Inc.

Cinnaminson, NJ7 decisions1980–19920 recalls

FDA records 7 decisions for Medical Equipment Development Co., Inc. (Cinnaminson, NJ) from 1980 to 1992: 7 510(k) clearances. Most are in product codes GZT (Retractor, Self-Retaining, For Neurosurgery) and HAW (Neurological Stereotaxic Instrument). 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, neurology panel, where it files most

How often FDA has decided Medical Equipment Development Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Equipment Development Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Equipment Development Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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