45 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FORA COMFORTSCAN EAR THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
K121116
FDA UDI
Life Spine, Inc.·00190837016029·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016043·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016258·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776172091·Webster Needle Holder, tungsten carbide, delica...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690130024·Retaining Bolt, PS or PS-C Insert, Revision Tib...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450474259·
PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018
PEDICLE SCREW 7X50
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018
PEDICLE SCREW 5X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018
DETACHABLE MONOPOLAR EMG NEEDLE, MODELS 610-725, 610-737, 610-637, 610-744, 610-650, 610-570
FDA 510(k)
FDA Class 2
·Neurology
ACTIVON TULLE
FDA 510(k)
FDA Unclassified
·Unknown
M.U.S.T. RODS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026
PEDICLE SCREW PEDICLE SCREW 5X40
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024
M.U.S.T. POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024
MUST PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017
Widex
FDA UDI
Widex A/S·05706069886092·WIDEX MOMENT MRB0 (Tech Black ) 220, RIC 10
Widex
FDA UDI
Widex A/S·05706069812343·Widex EVOKE E-PA (Tech Black ) 220, RC coil
PEDICLE SCREW - PEDICLE SCREW 8X75MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·October 11, 2018
PEDICLE SCREW PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·September 9, 2022