FDA Device Intelligence
HomeAROBELLA MEDICAL, LLC › Qoustic Wound Therapy System®, Qoustic Qurette® Probe, Type 13

Qoustic Wound Therapy System®, Qoustic Qurette® Probe, Type 13

AROBELLA MEDICAL, LLC · Model AR1000D · UDI-DI 00853077002176

NRBLFL Prescription
2
510(k) clearances
22
Adverse events (1 deaths)
0
Recalls
10
Facilities

Description

Qoustic Wound Therapy System®, Qoustic Qurette® Probe, Type 13 + Qoustic Qurette® Shroud, Type PWD

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.