FDA applicant

Pedro Aleman

D.F. Mexico, MX1 decision1985–19850 recalls

FDA records 1 decision for Pedro Aleman (D.F. Mexico, MX) in 1985: 1 510(k) clearance. All are in product code ILS (Adaptor, Hygiene). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Pedro Aleman since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pedro Aleman

Which product codes does it file in?

What has FDA decided for it lately?