510(k) Report

FDA applicant

Medsurg Industries, Inc.

Herndon, VA41 decisions1982–19940 recalls

FDA records 41 decisions for Medsurg Industries, Inc. (Herndon, VA) from 1982 to 1994: 41 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and LRO (General Surgery Tray). 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 Medsurg Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medsurg Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medsurg Industries, 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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