76 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FACTOR IX DEFICIENT PLASMA
FDA 510(k)
FDA Class 2
·Hematology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867050501·LO-PRO SCRW,TI,3.5MMX 24MM
PIVIT A/B ST AND PIVIT A/B ST-R
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SI-BONE iFuse Implant System®
FDA 510(k)
FDA Class 2
·Orthopedic
UNKNOWN DEPUY PINNACLE METAL LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 25, 2014
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·November 8, 2010
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·January 2, 2013
LO-PRO SCRW,TI,3.5MMX 24MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·August 13, 2025
DIST HUM FRAC PLT,EA,TI,LFT,11H,STRL
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRS·August 13, 2025
LO-PRO SCRW,TI,3.5MMX 28MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·September 10, 2018
LO-PRO SCRW,TI,3.5MMX 18MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·September 10, 2018
LO-PRO SCRW,TI,3.5MMX 22MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·September 10, 2018
LO-PRO SCRW,TI,3.5MMX 24MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·September 10, 2018
PLANTAR LAPIDUS PLATE, STANDARD RIGHT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 10, 2018
LOCKING SCREW, TITANIUM 3.5MM X 22MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 26MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 38MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 30MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019
CALCANEAL FRAC PERIMETER PLT,XS,RT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·April 18, 2019
LO-PRO SCRW,TI,3.5MMX 24MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·April 18, 2019