510(k) Report

FDA applicant

Life Medical Sciences, Inc.

New York, NY3 decisions1993–19980 recalls

FDA records 3 decisions for Life Medical Sciences, Inc. (New York, NY) from 1993 to 1998: 3 510(k) clearances. Most are in product codes MDA (Elastomer, Silicone, For Scar Management) and GAG (Stapler, 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 Life Medical Sciences, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Life Medical Sciences, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Life Medical Sciences, 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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