9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System
FDA 510(k)
FDA Class 2
·Orthopedic
NEXTAR INFRARED CAMERA
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021
METRON-CP/MD
FDA 510(k)
FDA Class 2
·Radiology
RETROFLEX DILATOR KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
EDWARDS ESHEATH INTRODUCER SET
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·December 6, 2021
EDWARDS TF SHEATH UNKNOWN
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·October 30, 2021
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CRMD·Product code NVN·January 13, 2014
UNKNOWN M2A MAGNUM HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 27, 2013
QUANTUM TTC ESOPHAGEAL BALLOON DILATOR
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KNQ·July 13, 2011