588 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FAQ 101
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Altus Spine Interbody Fusion System
FDA UDI
Altus Spine, LLC·00843210131610·Broach Trial
OsteoMed
FDA UDI
OSTEOMED LLC·00845694020800·FPS 2.0mm x 12mm Locking Screw
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193100128·EVOS Straight HA PEEK 12mm x 9mm x 22mm Biconve...
Caplugs/Evergreen
FDA UDI
CAPlugs·00810044204605·TEST TUBE 12X75MM
OsteoMed
FDA UDI
OSTEOMED LLC·00845694075121·FPS 2.0 x 12mm Locking Screw Sterile Qty 5
Z-MED Z-MED II
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES LOW PROFILE NEURO SYSTEM
FDA 510(k)
FDA Class 2
·Dental
INVACARE MEDICAL
FDA Adverse Event
Other
·DANYANG JUMAO HEALTHCARE EQUIPMENT CO.,LTD.·Product code IOR·October 26, 2012
MODULAR ANALYTICS CORE
FDA Adverse Event
Injury
·HITACHI HIGH TECH. CORP.·Product code JJE·November 6, 2008
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013
ACRYSOF IQ TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·February 24, 2012
ALARIS PCA UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 7, 2021
BED, AC-POWERED ADJUSTABLE HOSPITAL
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FNL·August 12, 2023
COMPLETE SE BILIARY SELF-EXPENDING STENT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code FGE·March 18, 2011
INTEGRA TISSUE EXPANDER
FDA Adverse Event
Other
·PMT CORP.·Product code LCJ·June 5, 2012
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·April 4, 2012
ARCHITECT CA 125 II
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LTK·December 5, 2012
STERIS STRETCHER
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FPO·August 12, 2023