14 results · 27ms · Sources: EU EUDAMED, US FDA

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FAMILY FITNESS SHIATSU MASSAGER

FDA 510(k)
FDA Class 1 ·Physical Medicine

TRANSEND EX 14 GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009

QBC(R) CENTRIFUGAL HEMATOLOGY CONTROL/MULTIPLE

FDA 510(k)
FDA Class 2 ·Hematology

WHITESIDE ACRYLIC CEMENT SPACER SLEEVE

FDA 510(k)
FDA Class 3 ·Unknown

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FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

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FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

ACUSON

FDA Adverse Event
Malfunction ·SIEMENS MEDICAL SOLUTIONS USA INC.·Product code IYN·May 5, 2014

HARMONIC ACE CURVED SHEARSINSERT ACCESSORY

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 5, 2013

EASYTRAK 2

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code OJX·January 3, 2011

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FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010

OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·October 13, 2021