FDA Device Intelligence
Home › Neuropace, Inc. › Wand

Wand

Neuropace, Inc. · Model W-02 · UDI-DI 00855547005113

PFN Prescription
0
510(k) clearances
746
Adverse events (2 deaths)
0
Recalls
3
Facilities

Description

The Wand package contains 1 Wand.

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.