207 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MAXIM SURGICAL X-TREME INTERBODY FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Unity Total Knee System
FDA UDI
CORIN LTD·05055343897744·Tibial Augment 5mm RM-LL size 3
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756612647·Wrist Splint
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813865·GENUMEDI PRO SILVER SIZE VI
TAPERLOC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304282223·
K2M General Instruments
FDA UDI
VB Spine LLC·10888857580213·Driver Shaft
SPERM CRYOPROTEC
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RAUMEDIC- ICP-MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 21, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
BIOLOX DELTA MODULAR CERAMIC HEAD 36MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·December 30, 2016
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 20, 2025
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026