FDA applicant

Coeur, Inc.

Lebanon, TN14 decisions2005–20170 recalls

FDA records 14 decisions for Coeur, Inc. (Lebanon, TN) from 2005 to 2017: 14 510(k) clearances. Most are in product codes DXT (Injector And Syringe, Angiographic) and DQX (Wire, Guide, Catheter). Its devices cite 40 predicates, 6 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2017

2007high 3 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Coeur, 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 “Coeur”

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

Coeur Laboratories, Inc. 10 Coeur Medical 1

Coeur, Inc.

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 “Coeur”