10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IODOSORB GEL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MODIFIED PGL ABSORBABLE STAPLE*
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
THERMOPROBE 210
FDA 510(k)
FDA Class 2
·Anesthesiology
G7 HI-WALL E1 LINER 36MM F
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LZO·January 10, 2019
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 10, 2022
DASHER -14 STEERABLE GUIDEWIRE
FDA Adverse Event
Injury
·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQX·January 9, 2007
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 28, 2020
HEARTSTART SLA BATTERY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code DQA·June 10, 2014
ACCENT DR RF
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 9, 2013
SYNCHRON CX9 ALX CLINICAL SYSTEM (RECONDITIONED)
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·November 22, 2010