34 results · 32ms · Sources: EU EUDAMED, 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