FDA applicant

Zimmer Cas

Montreal, CA3 decisions2011–20142 recalls

FDA records 3 decisions for Zimmer Cas (Montreal, CA) from 2011 to 2014: 3 510(k) clearances. Most are in product codes OLO (Orthopedic Stereotaxic Instrument) and KWS (Prosthesis, Shoulder, Semi-Constrained…). Its devices cite 5 predicates, 0 of them its own earlier devices. 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

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

FDA decisions per year

1in 2014

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

1in 2022

2011high 1 (2011) · low 0 (2012)2026

Class I Class II/III not classified

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

Planning a device like Zimmer Cas’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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Other applicant names beginning “Zimmer”

FDA records each applicant name separately; these may or may not be the same firm.

Zimmer, Inc. 426 Zimmer Spine, Inc. 44 Zimmer Dental, Inc. 40 Zimmer Biomet Spine, Inc. 15 Zimmer Medizinsysteme GmbH 13 Zimmer Trabecular Metal Technology 13 Zimmer Elektromedizin GmbH 12 Zimmer Trabecular 10 Zimmer Biomet 6 Zimmer Switzerland Manufacturing GmbH 4 Zimmer Patient Care Division 3 Zimmer Medizinsystems GmbH 2

Zimmer Cas

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?

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Other applicant names beginning “Zimmer”