646 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TheraBase, TheraBase Ca
FDA 510(k)
FDA Class 2
·Dental
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260384·
Bernafon
FDA UDI
Bernafon AG·05711584086810·ZR3, KIT 312 NFM 75 L BE ZERENA 3
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463066·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019040·2.0mm x 7mm Cannulated Lag Screw
CETRA
FDA UDI
Orthofix US LLC·18257200137435·CETRA - 2.0 SCREW CADDY, SEMI-CONSTRAINED SCREWS
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070065·Cannulated 2.0 x 7mm Lag Screw Sterile Qty 5
CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.2
FDA 510(k)
FDA Class 2
·Cardiovascular
PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
FDA 510(k)
FDA Class 2
·Anesthesiology
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·May 11, 2007
ACRYSOF
FDA Adverse Event
Injury
·ALCON LABORATORIES, INC/HUNTINGTON·Product code HQL·December 19, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·January 31, 2007
ENDO GIA ROTICULATOR 60-3. 5 SULU
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GAG·February 1, 2007
SYNCHROMED EL
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·May 31, 2007
ACRYSOF
FDA Adverse Event
Injury
·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·March 21, 2007
PINN MAR +4NEUT 32IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 6, 2008
UNK ZIMMER HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LZO·June 20, 2013
ADVANIX¿ BILIARY STENT WITH NAVIFLEX¿ RX DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code FGE·August 4, 2011
SYNTHETIC SLING MESH
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·April 18, 2007
6.5MM TWINFIX AB SUTURE ANCHOR W/NEEDLES
FDA Adverse Event
Malfunction
·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code MBI·January 23, 2008