FDA applicant

Progressive Surgical Products, Inc.

Westbury, NY3 decisions1994–19980 recalls

FDA records 3 decisions for Progressive Surgical Products, Inc. (Westbury, NY) from 1994 to 1998: 3 510(k) clearances. All are in product code MKY (System, Skin Closure). 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 Progressive Surgical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Progressive Surgical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Progressive”

FDA records each applicant name separately; these may or may not be the same firm.

Progressive Electrical Therapeutics 10 Progressive Dynamics, Inc. 7 The Progressive Orthopaedic Company, LLC 5 Progressive Medical Technology, Inc. 5 Progressive Concepts, Inc. 4 Progressive Productions, Ltd. 4 Progressive Technology, Inc. 3 Progressive Wound Care Technologies, LLC 1 Progressive Affiliated Labs, Inc. 1 Progressive Medical, Inc. 1 Progressive Iv'S, Inc. 1 Progressive Optical Research, Ltd. 1

Progressive Surgical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Progressive”