15 results · 24ms · Sources: EU EUDAMED, US FDA

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Gnesis EMS Plus

FDA 510(k)
FDA Class 2 ·Physical Medicine

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776182724·LEKSELL RONG SLIGHT-CVD

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780382775·Integra® Jarit® Leksell Rongeur, 9-1/4", 8mm Bi...

Intrigue

FDA UDI
LANCER ORTHODONTICS, INC.·00817573020591·INTRG WHISP-Z MBT 1BIC HK -12T 0A 018 LR

devemed

FDA UDI
devemed GmbH·04061644020836·Atraumatic tweezers, micro "Cooley" 0.8 mm, ang...

Reprocessed Inquiry Steerable Diagnostic EP Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

BATTERY, RECHARGEABLE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Reicodent

FDA UDI
devemed GmbH·04061644063130·Atraumatic tweezers, micro "Cooley" 0.8 mm, ang...

LEKSELL RONGEURS, 9", SLIGHT CURVE, 8MM BITE

FDA Adverse Event
Malfunction ·KAPP GMBH·Product code HTX·March 30, 2006

LEKSELL RONG 9 SLIGHT-CVD 8MM

FDA Adverse Event
Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code HTX·December 30, 2022

DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·September 10, 2024

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 22, 2015

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP·Product code LGW·November 13, 2008

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 16, 2013