FDA applicant

Ceramisys, Ltd.

Centercille, MA2 decisions2011–20110 recalls

FDA records 2 decisions for Ceramisys, Ltd. (Centercille, MA) in 2011: 2 510(k) clearances. Most are in product codes LYC (Bone Grafting Material, Synthetic) and HPZ (Implant, Eye Sphere). Its devices cite 3 predicates, 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, dental panel, where it files most

How often FDA has decided Ceramisys, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2011

2011high 2 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Ceramisys, Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Ceramisys, Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?