12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HD LifeSciences Cervical IBFD System
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517575913·CoRoent Ant TLIF Ti, 8x10x36mm 4°
Maestro™ Total Wrist
FDA UDI
Biomet Orthopedics, LLC·00887868239847·
MAESTRO TOTAL WRIST
FDA UDI
Biomet Orthopedics, LLC·00880304481114·
BYTE DAY ALIGNERS
FDA Adverse Event
Malfunction
·STRAIGHT SMILE, LLC·Product code NXC·October 31, 2024
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197081139·MASSON needle holder,straight
27 cm,...
GAMBRO CARTRIDGE BLOOD SET LOW WEIGHT- LOW VOLUME, MODEL 003422-520
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FINDRWIRZ GUIDE WIRE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DXY·May 13, 2019
HUDSON CONCHA NEPTUNE
FDA Adverse Event
Malfunction
·TELEFLEX·Product code BTT·October 15, 2014
GYNECARE PROSIMA PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·June 20, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 27, 2011