FDA applicant

Ed. Geistlich Soehne AG Fuer Chemische Industrie

Washington, DC6 decisions2003–20100 recalls

FDA records 6 decisions for Ed. Geistlich Soehne AG Fuer Chemische Industrie (Washington, DC) from 2003 to 2010: 6 510(k) clearances. Most are in product codes NPL (Barrier, Animal Source, Intraoral) and NPM (Bone Grafting Material, Animal Source). Its devices cite 15 predicates, 8 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, dental panel, where it files most

How often FDA has decided Ed. Geistlich Soehne AG Fuer Chemische Industrie’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ed. Geistlich Soehne AG Fuer Chemische Industrie by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Ed. Geistlich Soehne AG Fuer Chemische Industrie

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?