FDA applicant

Iberhospitex, S.A.

Barcelona, Spain, ES3 decisions1988–19890 recalls

FDA records 3 decisions for Iberhospitex, S.A. (Barcelona, Spain, ES) from 1988 to 1989: 3 510(k) clearances. Most are in product codes GCY (Apparatus, Suction, Single Patient Use…) and NAD (Dressing, Wound, Occlusive). 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 Iberhospitex, S.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Iberhospitex, S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Iberhospitex, S.A.

Which product codes does it file in?

What has FDA decided for it lately?