28 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Oticon
FDA UDI
Oticon A/S·05707131260536·RIA PRO, RITE 312 WL DBL
Humelock Reversed Shoulder
FDA UDI
FX SOLUTIONS·03701037301395·HUMELOCK REVERSED STEM TA6V CEMENTED Ø32/08
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1671332080·
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019
REVERSE SHOULDER PROSTHESIS MONOBLOCK STEM
FDA 510(k)
FDA Class 2
·Orthopedic
IVY DEVICES INC. IV/MEDICAL LINE STABILIZER
FDA 510(k)
FDA Class 2
·General Hospital
CLYDESDALE PTC SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019
FREESTYLE FREEDOM
FDA Adverse Event
Malfunction
·Product code NBW·May 29, 2013
4MM A/C CANNULA, 2 ROTATING STOPCOCKS W/SPEEDLOCK
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code DWF·May 9, 2011
RF 3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code GEI·August 22, 2008
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023
DENALI FEMORAL SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023
DENALI FEMORAL SYSTEM
FDA Adverse Event
Injury
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 20, 2023
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 26, 2023
DENALI FEMORAL SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 6, 2023
DENALI FEMORAL SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 20, 2023