FDA applicant

Internacional Farmacéutica S.A DE C.V

Lerma, MX1 decision2025–20250 recalls

FDA records 1 decision for Internacional Farmacéutica S.A DE C.V (Lerma, MX) in 2025: 1 510(k) clearance. All are in product code GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid). Its devices cite 1 predicate, 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, general and plastic surgery panel, where it files most

How often FDA has decided Internacional Farmacéutica S.A DE C.V’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2025high 1 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Internacional Farmacéutica S.A DE C.V by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Internacional Farmacéutica S.A DE C.V’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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Other applicant names beginning “Internacional”

FDA records each applicant name separately; these may or may not be the same firm.

Internacional Farmaceutica, S.A. DE C.V. 10

Internacional Farmacéutica S.A DE C.V

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Internacional”