FDA applicant

Rhino Metrics A/S

Minneapolis, MN2 decisions2000–20020 recalls

FDA records 2 decisions for Rhino Metrics A/S (Minneapolis, MN) from 2000 to 2002: 2 510(k) clearances. All are in product code BXQ (Rhinoanemometer (Measurement Of Nasal…). Its devices cite 1 predicate, 0 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, anesthesiology panel, where it files most

How often FDA has decided Rhino Metrics A/S’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rhino Metrics A/S since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rhino Metrics A/S by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Rhino”

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

Rhino Health, Inc. 3 Rhino Mfg. 2

Rhino Metrics A/S

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 “Rhino”