2,250 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RADIOLOCENT DRIVE DRILL BIT
FDA Adverse Event
Malfunction
·STRYKER IRELAND LTD.·Product code GFF·July 12, 2011
BURR, OVAL, 8 FLUTE 4.0MM X 13CM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GFF·October 4, 2018
4.5MM STERLING LIGHTNING BUR
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code GFF·October 9, 2018
BURR, OVAL, 12 FLUTE 5.5MM X 13CM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GFF·November 29, 2018
BUR,OVAL,FLUSHCUT,6 FLUT,5.MMX 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·September 12, 2023
BURR, ROUND, 8 FLUTE 5.0MM X 13VM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·August 16, 2023
4.5MM X 19CM HPS PREBENT POLISHING BUR
FDA Adverse Event
Malfunction
·CONMED LARGO·Product code GFF·August 11, 2023
4.0MM ROUND SOLID CARBIDE BUR LONG
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·July 26, 2023
2.2MM LINDEMANN DRILL BIT
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·July 26, 2023
BUR,OVAL,FLUSHCUT,12 FLUT,5.0MMX 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·August 11, 2023
BUR, SURGICAL, GENERAL AND PLASTIC SURGERY
FDA Adverse Event
Malfunction
·BRASSELER·Product code GFF·August 12, 2023
BUR,OVAL,CLEARCUT,8 FLUT,5.0MMX 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·September 28, 2023
POWERASP,4.0MM X 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·July 18, 2023
1.1MM DRILL BIT/MINI QC/45MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code GFF·September 12, 2023
POWERASP,4.0MM X 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·August 4, 2023
BURR, OVAL, 8 FLUTE 5.0MM X 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·September 18, 2023
2.2MM LINDEMANN DRILL BIT
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code GFF·October 28, 2025
BUR,RND,CLEARCUT,8 FLUT,5.5MMX 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·October 7, 2025
BUR,RND,CLEARCUT,8 FLUT,5.5MMX 13CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·October 7, 2025
BUR,RND,SJ,8 FLUT 3.0MMX 7CM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code GFF·September 22, 2025