31 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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YUKON OCT Spinal System
FDA 510(k)
FDA Class 2
·Orthopedic
VeriQuick
FDA UDI
FOURSTAR GROUP INC.·00049696609531·
Ambler Value Line
FDA UDI
AMBLER SURGICAL CORP.·00190660214210·Deaver retractor, 12'' long x 2'' wide blade, f...
MECHANICAL WHEELCHAIR - L-FRAME SERIES
FDA 510(k)
FDA Class 1
·Physical Medicine
AUTOSUTURE ENDO GIA SINGLE USE TAN RELOAD WITH TRI-STAPLE TECHNOLOGY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151979·17 X 14 CERVICAL TRIALS 44MM 0° LORDOSIS
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606152167·17 X 14 CERVICAL TRIALS 44MM 10° LORDOSIS
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
VC10 PUMP, 115V
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code HHK·January 2, 2025
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
COMMUNICATOR
FDA Adverse Event
Malfunction
·EXTERNAL MANUFACTURER·Product code LWS·July 21, 2011