1,800 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 21, 2022
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 21, 2022
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 12, 2022
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 12, 2022
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·June 6, 2022
MOD ARTHRO 5 DEG LCK COLLAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSB·June 7, 2021
VG CR MONO-LCK BRG 12X75
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·July 19, 2024
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·September 19, 2024
4.5MM LCK COMP PL 10H 193MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HRS·October 12, 2018
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018
3.5MM LCK TUBULAR PL 6H 82MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HRS·October 30, 2018
4.5MM LCK COMP PL 12H 229MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HRS·December 19, 2018
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·November 13, 2025
VANGUARD CR MONO-LCK BEARING 10X71
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·March 8, 2013
2.7MM VA LCK SCREW SLF-TAP
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018
MINICTH VSYS/PRT/LCK 4NDL LWPF
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL·Product code LJT·April 25, 2013
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·November 13, 2025
BIO-COMP-SITE P-LCK 2.9X15.5MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·October 16, 2025