510(k) Report

FDA applicant

Alandra Medical Sapi DE CV

Mexico City, MX1 decision2024–20240 recalls

FDA records 1 decision for Alandra Medical Sapi DE CV (Mexico City, MX) in 2024: 1 510(k) clearance. All are in product code QIS (Esophageal, Mucosal, Electrical Characterization). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, gastroenterology and urology panel, where it files most

How often FDA has decided Alandra Medical Sapi DE CV’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024: 1
2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Alandra Medical Sapi DE CV by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Alandra Medical Sapi DE CV’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • QISEsophageal, Mucosal, Electrical Characterization1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K233974Mucosal Impedance Measurement SystemAlandra Medical Sapi DE CV · 2024

The one decision as Alandra Medical Sapi DE CV →