31 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANKYLOS DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SOAR Retractor System
FDA UDI
SPINEOLOGY INC.·M7403041509·15mm x 90mm Portal Tube
STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE
FDA 510(k)
FDA Class 2
·Cardiovascular
BARRETT UNICONDYLAR TIBIAL BEARING
FDA 510(k)
FDA Class 2
·Orthopedic
DYNASTY(R) COCR LINER
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 10, 2018
UNKNOWN
FDA Adverse Event
Malfunction
·COOK, INC.·Product code DTK·August 21, 2014
UNK
FDA Adverse Event
Injury
·COOK, INC.·Product code DTK·August 20, 2014
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·August 20, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 24, 2011
CONTAK RENEWAL 3
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008
GUNTHER TULIP VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·April 3, 2026
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·December 5, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·November 1, 2017
GUNTHER TULIP VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·November 4, 2025
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·February 27, 2018
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·May 5, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·May 12, 2017
UNKNOWN
FDA Adverse Event
Injury
·Product code DTK·August 20, 2020
UNK
FDA Adverse Event
Injury
·COOK, INC.·Product code DTK·August 20, 2014