510(k) Report

FDA applicant

Symatese

Chaponost1 decision2025–20250 recalls

FDA records 1 decision for Symatese (Chaponost) in 2025: 1 original PMA approval. All are in product code LMH (Implant, Dermal, For Aesthetic Use). 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 Symatese’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2025: 1
2025high 1 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Symatese by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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