FDA Device Intelligence
Home › SANUWAVE Health, Inc. › UltraMIST Treatment Wand

UltraMIST Treatment Wand

SANUWAVE Health, Inc. · Model CP-80033 · UDI-DI 00812265010324

NRB
1
510(k) clearances
22
Adverse events (1 deaths)
0
Recalls
10
Facilities

Description

Component to the UltraMIST System

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.