510(k) Report

FDA applicant

Medical Sterilization, Inc.

Unnamed device, NY6 decisions1984–19990 recalls

FDA records 6 decisions for Medical Sterilization, Inc. (Unnamed device, NY) from 1984 to 1999: 6 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) and FYA (Gown, Surgical). 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 Sterilization, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Sterilization, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Sterilization, 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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