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

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Reveal LINQ

FDA 510(k)
FDA Class 2 ·Cardiovascular

BONASTENT® Tracheal/Bronchial

FDA UDI
Sewoon Medical Co., Ltd.·08806369468947·

B-P TOTAL HIP SYSTEM

FDA UDI
ENDOTEC, INC.·00814193024640·B-P MODULAR EXTENSION W/ULTRACOAT - 9 MM X 200 MM

OSTEO-LINK BONE VOID FILLER PELLETS

FDA 510(k)
FDA Class 2 ·Orthopedic

WIRELESS MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·May 31, 2017

CAPSUREFIX

FDA Adverse Event
Injury ·MPRI·Product code NVN·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

UNKNOWN ZIMMER HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·July 7, 2011

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·May 7, 2018

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017