FDA applicant

Cvrx, Inc.

Minneapolis1 decision2019–20190 recalls

FDA records 1 decision for Cvrx, Inc. (Minneapolis) in 2019: 1 original PMA approval. All are in product code DSR (Stimulator, Carotid Sinus Nerve). 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 Cvrx, 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 — Cvrx, Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cvrx, 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

Cvrx, Inc.

Which product codes does it file in?

What has FDA decided for it lately?