34 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Performer Guiding Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
PERFORMER MULLINS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 20, 2023
PERFORMER MULLINS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 24, 2024
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·November 4, 2022
PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X40MM LOT. 1
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2019
HEAL FORCE CO2 INCUBATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EASYSCAN MODEL 1.2
FDA 510(k)
FDA Class 2
·Ophthalmic
M.U.S.T. POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X30MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·May 14, 2024
PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 7X35MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·March 10, 2021
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 14, 2013
PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X35MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2023
M.U.S.T. RODS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·March 31, 2026
MYSPINE MC DRILL BASED GUIDE L05
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PQC·December 10, 2019
MECTALIF OBLIQUE (TI PEEK) TIPEEK 10X24X10 L5°
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·June 25, 2024
ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 5X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·January 10, 2024
PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 5X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·July 25, 2023
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC·Product code JJE·July 15, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013
PROLENE OR % -AS LISTED WITH THE FDA-
FDA Adverse Event
Injury
·ETHICON·Product code FTL·September 22, 2008