FDA applicant

Zimmer Patient Care Division

Dover, OH3 decisions1993–19960 recalls

FDA records 3 decisions for Zimmer Patient Care Division (Dover, OH) from 1993 to 1996: 3 510(k) clearances. Most are in product codes FMQ (Restraint, Protective) and CAC (Apparatus, Autotransfusion). 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 Patient Care Division’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zimmer Patient Care Division since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Cas 3 Zimmer Medizinsystems GmbH 2

Zimmer Patient Care Division

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Zimmer”