510(k) Report

FDA applicant

Hindernis DE Mexico, S.A.P.I. DE C.V.

Naucalpan De Juarez, MX1 decision2026–20260 recalls

FDA records 1 decision for Hindernis DE Mexico, S.A.P.I. DE C.V. (Naucalpan De Juarez, MX) in 2026: 1 510(k) clearance. All are in product code FYA (Gown, Surgical). 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 Hindernis DE Mexico, S.A.P.I. DE C.V.’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 — Hindernis DE Mexico, S.A.P.I. DE C.V. by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hindernis DE Mexico, S.A.P.I. 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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