43 results
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28ms
·
Sources: EU EUDAMED, US FDA
ACUITY CENTRAL STATION, MODEL 020XXXXX (NOTE: XXXXX = VARIOUS CONFIG.)
FDA 510(k)
FDA Class 2
·Cardiovascular
Armada
FDA UDI
Nuvasive, Inc.·00887517209511·ARM15T Rod, 160mm Conventional Pre-Bent
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809849813·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE SMALL KH...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192206·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981173876·L Con, Side-Loading, R, 16mm, 160mm
XIA SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COMPCORE AF COMPOSITE CORE BUILD-UP MATERIAL, MODEL 3001408
FDA 510(k)
FDA Class 2
·Dental
SLEEPEASY
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·April 12, 2012
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 6, 2010
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 25, 2009
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·November 28, 2019
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·January 6, 2021
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·May 22, 2018
EXT DRAINAGE SYSTEM III WITHOU VENT CATH
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·April 11, 2013
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 12, 2011