24 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCUFLATE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
NuVasive
FDA UDI
Nuvasive, Inc.·00887517390974·CoRoent XLW Trial, 12x22x50mm 10°
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902930300·INSTRUMENT 8910512 ALIF TRIAL 12MM
ZAVATION
FDA UDI
Zavation LLC·00842166151703·WHITNEY 13mmx15mm , 5deg , 12mm
UCR
FDA UDI
Seaspine Orthopedics Corporation·10889981079994·4MM HEX SHAFT
SmartBand EMR Kit, SmartBand EMR Pack, SmartSnare
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SIMMETRY SACROILIAC JOINT FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·September 27, 2019
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 30, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·July 2, 2014
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·November 30, 2012
BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·March 20, 2023
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·December 5, 2017
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·June 25, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 23, 2017
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 3, 2017
BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·November 4, 2025
BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·January 11, 2023
BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·September 9, 2022
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·September 8, 2017