510(k) Report

FDA applicant

Desarrollo e Investigación Médica Aragonesa S.L.

Calatayud, ES1 decision2026–20260 recalls

FDA records 1 decision for Desarrollo e Investigación Médica Aragonesa S.L. (Calatayud, ES) in 2026: 1 510(k) clearance. All are in product code OTN (Mesh, Surgical, Synthetic, Urogynecologic, For…). 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 Desarrollo e Investigación Médica Aragonesa S.L.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026 (partial year): 1
2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

FIG. 1 — Desarrollo e Investigación Médica Aragonesa S.L. by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OTNMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic…1decision

What has FDA decided for it lately?

  • K262284Kim BlueDesarrollo e Investigación Médica Aragonesa S.L. · 2026

The one decision as Desarrollo e Investigación Médica Aragonesa S.L. →