FDA Device Intelligence
Home › NANOVIBRONIX INC. › PainShield 3.0 Actuator

PainShield 3.0 Actuator

NANOVIBRONIX INC. · Model 3.0 · UDI-DI 07290103421144

PFW Prescription
9
510(k) clearances
2
Adverse events
0
Recalls
11
Facilities

Description

PainShield actuator is part of the PainShield MD 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.