87 results · 19ms · Sources: EU EUDAMED, US FDA

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PrimeLOC Attachment System

FDA 510(k)
FDA Class 2 ·Dental

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA UDI
FX SOLUTIONS·03701037317976·TRIAL HUMERAL CUP ECCENTRIC SYMMETRIC MOBILITY ...

Zavation

FDA UDI
Zavation LLC·00842166132887·Ti3Z CIF 14mmx16mmx12mm -6 deg

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113379·PS Insert, Size 6 x 12mm

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220612070·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220612150·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220612000·

SilverGlide

FDA UDI
STRYKER CORPORATION·04546540696038·ProSeries Non-stick Bipolar Electrosurgical For...

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT

FDA 510(k)
FDA Class 2 ·Cardiovascular

SULTAN SPOROX TEST VIAL, MODEL 75195

FDA 510(k)
FDA Class 2 ·General Hospital

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 12, 2024

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024