510(k) Report

FDA applicant

Sentienx Sdn Bhd

Kulim, MY1 decision2023–20230 recalls

FDA records 1 decision for Sentienx Sdn Bhd (Kulim, MY) in 2023: 1 510(k) clearance. All are in product code KGO (Surgeon'S Gloves). 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 Sentienx Sdn Bhd’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023: 1
2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Sentienx Sdn Bhd by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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