FDA applicant

Cornelia Damsky, Inc.

Stamford, CT4 decisions1985–20000 recalls

FDA records 4 decisions for Cornelia Damsky, Inc. (Stamford, CT) from 1985 to 2000: 4 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) and GEX (Powered Laser Surgical Instrument). 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 Cornelia Damsky, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cornelia Damsky, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cornelia Damsky, Inc.

Which product codes does it file in?

What has FDA decided for it lately?