28 results · 23ms · Sources: EU EUDAMED, 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