FDA applicant

Dove Medical Supplies

Vancouver, WA2 decisions1987–19880 recalls

FDA records 2 decisions for Dove Medical Supplies (Vancouver, WA) from 1987 to 1988: 2 510(k) clearances. Most are in product codes KPO (Dialysate Concentrate For Hemodialysis (Liquid…) and FKG (Tray, Start/Stop (Including Contents), Dialysis). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Dove Medical Supplies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dove Medical Supplies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dove Medical Supplies’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 “Dove”

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

Dove Systems, Inc. 1

Dove Medical Supplies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dove”