29 results · 22ms · Sources: EU EUDAMED, US FDA

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BioPhotas Celluma3

FDA 510(k)
FDA Class 2 ·Physical Medicine

CoRoent

FDA UDI
Nuvasive, Inc.·00887517566393·CoRoent Ant TLIF PEEK, 15x12x28mm 0°

Epimed

FDA UDI
EPIMED INTERNATIONAL, INC·00818788020406·22g TW x 8.0" Chiba Style Needle w/ Introducer

FILTERWIRE EZ EMBOLIC PROTECTION SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

STRAUMANN CARES SCREW-RETAINED BRIDGE TITANIUM, STRAUMANN CARES DOLDER BAR TITANIUM

FDA 510(k)
FDA Class 2 ·Dental

ANTHEM RF

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

SCANNER TAG

FDA Adverse Event
Malfunction ·SURGICOUNT·Product code LWH·July 2, 2011

SECURA DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

METACROSS OTW PTA BALLOON DILATATION CATHETER

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

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·December 26, 2019

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·July 19, 2019

PTA BALLOON CATHETER(OHICHO3)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

BD CONNECTA¿ 3-WAY STOPCOCK

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·September 12, 2023

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 31, 2025