19 results · 23ms · Sources: EU EUDAMED, US FDA

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SUB-TALAR LOK, MODEL 7-11 MM

FDA 510(k)
FDA Class 2 ·Orthopedic

AORTIC ROOT RETRACTOR

FDA UDI
LSI Solutions, Inc.·00850200006568·AORTIC ROOT RETRACTOR, LARGE

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014605524·MAQUET 1130 ORTHOPEDIC 2.25" DELUXE GEL

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450180594·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450182840·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450169636·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197500685·VATS MICS Chest Tube Passer WL 280...

PRECINORM PROTEINS IN URINE/CSF PRECIPATH PROTEINS IN URINE/CSR CONTROLS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

PULMOLAB EX671 EXERCISE TESTING SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

NEURAGEN NERVE GUIDE 2MM ID X 2CM LENGTH

FDA Adverse Event
Other ·INTEGRA LIFESCIENCES CORP.·Product code JXI·June 14, 2010

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

ALIGN URETHRAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code OTN·April 24, 2013

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 31, 2011

SYNERGY

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·July 22, 2008

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008

On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems, Inc.·April 30, 2014