FDA applicant

Mecron Medical Products, Inc.

Port Washington, NY14 decisions1984–19860 recalls

FDA records 14 decisions for Mecron Medical Products, Inc. (Port Washington, NY) from 1984 to 1986: 14 510(k) clearances. Most are in product codes KWL (Prosthesis, Hip, Hemi-, Femoral, Metal) and KTW (Appliance, Fixation, Nail/Blade/Plate…). 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, orthopedic panel, where it files most

How often FDA has decided Mecron Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mecron Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mecron Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?