FDA applicant

Rnk Products, Inc.

Burnsville, MN6 decisions2004–20130 recalls

FDA records 6 decisions for Rnk Products, Inc. (Burnsville, MN) from 2004 to 2013: 6 510(k) clearances. All are in product code DQD (Stethoscope, Electronic). Its devices cite 8 predicates, 5 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Rnk Products”.

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 Rnk Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2007high 2 (2013) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Rnk Products, 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?