FDA applicant

Zimmer Surgical, Inc.

Dover, OH1 decision2019–20190 recalls

FDA records 1 decision for Zimmer Surgical, Inc. (Dover, OH) in 2019: 1 510(k) clearance. All are in product code FYA (Gown, Surgical). 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 Zimmer Surgical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Zimmer Surgical, Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

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 Surgical, Inc.

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”