FDA applicant

Teoxane S.A.

Geneva1 decision2017–20170 recalls

FDA records 1 decision for Teoxane S.A. (Geneva) in 2017: 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 Teoxane S.A.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Teoxane S.A. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Teoxane S.A.

Which product codes does it file in?

What has FDA decided for it lately?