FDA applicant

Rmds, Inc.

Vancouver, WA4 decisions1997–19970 recalls

FDA records 4 decisions for Rmds, Inc. (Vancouver, WA) in 1997: 4 510(k) clearances. All are in product code DXC (Clamp, Vascular). 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 Rmds, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rmds, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Rmds, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?