38 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PICA WHOLE-BODY MRI SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Corin BiPolar-i
FDA UDI
CORIN LTD·05056139234569·Corin BiPolar-i Ø42/22mm
Copper Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989028799·COPPER NITI 40 BAF16X22LO SM PK10
Posted Stainless Steel Archwire
FDA UDI
Ortho Arch Company Inc·D90911094214·.019 X .025 POSTED SS RIGHT FORM WIRES 42MM (10)
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450159019·
U04
FDA 510(k)
FDA Class 2
·Radiology
U-RIGHT EAR THEMOMETER, MODELS TD-1115 AND TD-1118
FDA 510(k)
FDA Class 2
·General Hospital
PERCLOSE PROGLIDE
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code MGB·February 5, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 29, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·June 11, 2014
GENESIS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 8, 2013
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 11, 2014
LIGAMAX-5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 2, 2011
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 2, 2018
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 2, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 2, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2017
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NKB·May 6, 2022