510(k) Report

FDA applicant

Mr Associates, Inc.

Mchenry, IL15 decisions1980–19800 recalls

FDA records 15 decisions for Mr Associates, Inc. (Mchenry, IL) in 1980: 15 510(k) clearances. Most are in product codes OCZ (Endoscopic Grasping/Cutting Instrument…) and KNS (Unit, Electrosurgical, Endoscopic (With Or…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Mr Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mr Associates, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mr Associates, 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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