FDA applicant

Zimmer Aspen Labs

Englewood, CO1 decision1987–19870 recalls

FDA records 1 decision for Zimmer Aspen Labs (Englewood, CO) in 1987: 1 510(k) clearance. All are in product code BWA (Unit, Electrosurgical And Coagulation, With…). 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 Aspen Labs’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zimmer Aspen Labs since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Zimmer Aspen Labs 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 Patient Care Division 3 Zimmer Cas 3

Zimmer Aspen Labs

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Zimmer”