29 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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4-WEB CERVICAL STS (SPINAL TRUSS SYSTEM)
FDA 510(k)
FDA Class 2
·Orthopedic
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564032362·400 CC SMALL BASIN
Z Liquid ST C4-S 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121741·Dental porcelain/ceramic restoration kit
23 G X 1 IN. BD INTEGRA¿ 3 ML SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 7, 2017
23 G X 1 IN. BD INTEGRA¿ 3 ML SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·November 7, 2017
DIATRON PICTUS 400
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CRITERTION, MODEL #1067511
FDA 510(k)
FDA Class 2
·Dental
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 21, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014
WECK HEM-O-LOK ENDO APPLIER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code FZP·May 20, 2011
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 14, 2016
StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.
FDA Enforcement
Class II
·Terminated·Abbott Vascular·February 22, 2017
GYNECARE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTO·July 27, 2018
2210968-2018-74702
FDA Adverse Event
Injury
·July 29, 2018