FDA applicant

Condomi Erfert Prodoktionsgesellschaft Mbh

Great Neck, NY1 decision2002–20020 recalls

FDA records 1 decision for Condomi Erfert Prodoktionsgesellschaft Mbh (Great Neck, NY) in 2002: 1 510(k) clearance. All are in product code HIS (Condom). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Condomi Erfert Prodoktionsgesellschaft Mbh’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Condomi Erfert Prodoktionsgesellschaft Mbh since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Condomi Erfert Prodoktionsgesellschaft Mbh

Which product codes does it file in?

What has FDA decided for it lately?