589 results
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26ms
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Sources: EU EUDAMED, US FDA
CHIKAI Nexus petit
FDA 510(k)
FDA Class 2
·Cardiovascular
FPS
FDA UDI
Tyber Medical, LLC·00810040686252·Ø2.5mm Locking Screw, VA 11mm
TMS SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036089429·
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252011400·ceraMotion® Me Opaque C2, 40 g / dental ceramic...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197392921·Takahashi Suction Punch
3,5mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197392914·Takahashi Suction Punch
2,5mm,...
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918188546·Sponge Angled Blue and white prep stick_bulk p...
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252011200·ceraMotion® Me Opaque C2, 20 g / dental ceramic...
PILONPLATE WITH ANGULAR STABILITY
FDA 510(k)
FDA Class 2
·Orthopedic
Lucent Intervertebral Body Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
Exactech, Inc.·10885862523907·TRIAL, TIBIAL INSERT, SPACER, SIZE 0, 11mm
CNS-6201A
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·February 10, 2020
ACRYSOF IQ TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 7, 2011
ACRYSOF IQ TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 7, 2011
SYNERGY
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·December 4, 2008
ASR ACETABULAR IMPLANT 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·September 16, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 29, 2013
Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-664 Donor# B090056 2.5cc Expiration Date: 12/25/2011; LBL 210-0010-1 REV: 040109; and Graft ID# B090056-675. Bone void filler for voids or gaps in bone. Indicated for treatment of surgically created osseous defects. On 07/12/2012 an additional expired product was discovered by a Bacterin sales rep. B100078-908 with expiration date 04/27/2012
FDA Enforcement
Class II
·Terminated·Bacterin International, Inc.·February 20, 2013
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·March 25, 2011
PERMANENT PACEMAKER ELECTRODE
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code DTB·August 12, 2023