FDA applicant
Medical Equipment Development Co., Inc.
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
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.
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.
See the 510(k) Report