FDA Device Intelligence
Home › SENSEONICS, INCORPORATED › Eversense Power Adapter

Eversense Power Adapter

SENSEONICS, INCORPORATED · Model FG-6000-01-303 · UDI-DI 00817491023858

QHJ Prescription
0
510(k) clearances
2,485
Adverse events
1
Recalls
8
Facilities

Description

Power Adapter (i.e., wall plug)

Recalls

DateFirmReason
2019-09-18Senseonics, Inc.Eversense Sensors have prematurely stopped functioning due to inadequate hydration of the sensor s glucose-sensing surface

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.