FDA applicant

Ceterix Orthopaedics, Inc.

Fremont, CA3 decisions2015–20180 recalls

FDA records 3 decisions for Ceterix Orthopaedics, Inc. (Fremont, CA) from 2015 to 2018: 3 510(k) clearances. All are in product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene). Its devices cite 4 predicates, 2 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, general and plastic surgery panel, where it files most

How often FDA has decided Ceterix Orthopaedics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2018

2015high 2 (2018) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Ceterix Orthopaedics, Inc. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ceterix Orthopaedics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Ceterix Orthopaedics, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?