510(k) Report

FDA applicant

Medical Products Development, Inc.

Mchenry, IL13 decisions1980–19810 recalls

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, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

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.

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

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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