31 results
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30ms
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Sources: EU EUDAMED, US FDA
INTUITIVE SURGICAL DA VINCI S SURGICAL SYSTEM, MODEL IS2000, WITH DA VINCI CONNECT AND ONSITE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FortiFix
FDA UDI
NANOVIS SPINE, LLC·00814216026903·Nano FortiFix (S) Reduction screw module
VADER Pedicle System, Rod, Ti, Curved, Ø 6.0 r120 x 70 mm
FDA UDI
icotec AG·07640164847313·VADER Pedicle System, Rod, Ti, Curved, Ø 6.0 r1...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm
LASER PERIPHERALS REUSABLE HOLMIUM FIBER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STARLIGHT
FDA 510(k)
FDA Class 2
·Neurology
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 7, 2025
IPC® STYLUS TRANSNASAL BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·February 6, 2015
IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code ERL·June 19, 2015
XPS® BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·September 8, 2017
ACCY EF201 IPC FOOT CONTROL ROHS
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code HBE·September 9, 2014
XPS® BUR - UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code EQJ·June 17, 2016
1.25MM KIRSCHNER WIRE W/TROCAR POINT 150MM
FDA Adverse Event
Malfunction
·SYNTHES·Product code LRN·April 26, 2013
AXIEM PORTABLE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 21, 2011
SELF CENT HIP 49X28 BRN
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 23, 2008
XOM UNKNOWN ENDO
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code EQJ·May 8, 2015
XPS® HANDPIECE - UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code HBE·November 8, 2016
IPC® FOOTPEDAL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·March 1, 2016
XPS® HANDPIECE - UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code HBE·October 17, 2017