FDA applicant
Medical Products Development, Inc.
FDA records 13 decisions for Medical Products Development, Inc. (Mchenry, IL) from 1980 to 1981: 13 510(k) clearances. Most are in product codes HQP (Unit, Cautery, Thermal, Battery-Powered) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Products Development, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medical Products Development, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medical Products Development, 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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