FDA applicant

Zimmer Orthopaedic Surgical Products

Dover, OH1 decision2005–20050 recalls

FDA records 1 decision for Zimmer Orthopaedic Surgical Products (Dover, OH) in 2005: 1 510(k) clearance. All are in product code FRN (Pump, Infusion). Its devices cite 2 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Zimmer Orthopaedic Surgical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Zimmer Orthopaedic Surgical Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Zimmer Orthopaedic Surgical Products’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 Cas 3

Zimmer Orthopaedic Surgical Products

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?

Other applicant names beginning “Zimmer”