32 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Mikron Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY
FDA 510(k)
FDA Class 2
·Cardiovascular
ATLAS SPINE VERTEBRAL BODY REPLACEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 21, 2011
CD3200SL 110
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·September 17, 2008
COPE MANDRIL WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·September 9, 2021
COPE NITINOL MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·October 28, 2022
TORQ-FLEX AUSTRALIAN MODIFICATION MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·January 13, 2022
COPE MANDRIL WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·May 24, 2021
APPROACH CTO MICROWIRE WIRE GUIDE
FDA Adverse Event
Injury
·Product code DQX·May 21, 2021
APPROACH CTO MICROWIRE WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·December 28, 2021
COPE NITINOL MANDRIL WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·August 2, 2024
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
COPE NITINOL MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·May 16, 2022
COPE MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·August 19, 2021
COPE NITINOL MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·Product code DQX·August 10, 2021
COPE MANDRIL WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 27, 2022
COPE NITINOL MANDRIL WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code DQX·July 28, 2022