510(k) Report

FDA applicant

Savoy Medical Supply Co., Inc.

Hauppauge, NY7 decisions1993–19930 recalls

FDA records 7 decisions for Savoy Medical Supply Co., Inc. (Hauppauge, NY) in 1993: 7 510(k) clearances. Most are in product codes MDM (Instrument, Manual, Surgical, General Use) and KKX (Drape, Surgical, Antimicrobial). 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 Savoy Medical Supply Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Savoy Medical Supply Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Savoy Medical Supply Co., 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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