39 results · 39ms · Sources: EU EUDAMED, US FDA

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TZ SKULL PIN Adult

FDA 510(k)
FDA Class 2 ·Neurology

CoRoent

FDA UDI
Nuvasive, Inc.·00887517638564·CoRoent Ant TLIF PEEK, 16x13x32mm 12°

Archimed 627 Spinal Brace

FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357633227·

N.A.

FDA UDI
DENTAURUM GmbH & Co.KG·J011163322000·ConTec Go! disposable tube

DIMENSION VISTA TRF FLEX REAGENT CARTRIDGE, PROTEIN 1 CALIBRATOR PROTEIN 1 CONTROL L,CONTROL M, CONTROL H

FDA 510(k)
FDA Class 2 ·Immunology

EVERCROSS 0.035 OTW PTA DILATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

TRI-LOCK BPS SZ 3 STD OFFSET

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·July 8, 2011

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·October 10, 2014

IKAZUCHI ZERO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·June 13, 2019

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·August 19, 2019

IKAZUCHI ZERO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·August 20, 2019

KANEKA PTCA CATHETER CO-R7(IKAZUCHI ZERO)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·August 21, 2019

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code LOX·April 14, 2022

KANEKA PTCA CATHETER CO-R8 (TASUKI)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·December 13, 2020

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code LOX·December 21, 2020

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code LOX·April 13, 2022

TRANS-RAY PLUS 7.5FR 35CC IAB WITH ACCESSORIES

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·July 30, 2025