FDA applicant

Medicalex

Paris 75013, FR4 decisions1984–19850 recalls

FDA records 4 decisions for Medicalex (Paris 75013, FR) from 1984 to 1985: 4 510(k) clearances. Most are in product codes FQM (Bandage, Elastic) 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, general and plastic surgery panel, where it files most

How often FDA has decided Medicalex’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medicalex since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medicalex

Which product codes does it file in?

What has FDA decided for it lately?