36 results · 25ms · Sources: EU EUDAMED, US FDA

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Gelsoft™ Plus Vascular Prostheses

FDA 510(k)
FDA Class 2 ·Cardiovascular

MaXcess

FDA UDI
Nuvasive, Inc.·00887517197153·MaXcess 4 Blade, 70mm Left

SKYHAWK

FDA UDI
Orthofix US LLC·18257200085354·PLATE INSERTER

Spud

FDA UDI
KATENA PRODUCTS, INC.·00841668101223·ELLIS FOREIGN BODY SPUD

STRAUMANN TEMPORARY COPING

FDA 510(k)
FDA Class 2 ·Dental

SUPER SHEATH

FDA 510(k)
FDA Class 2 ·Cardiovascular

INTERSTIM

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 17, 2011

ROTALINK CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code MCX·November 20, 2008

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FPA·July 22, 2013

SUPERSHEATH

FDA Adverse Event
Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022

SUPERSHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018

SUPERSHEATH

FDA Adverse Event
Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020

SUPERSHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·February 11, 2020

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·January 19, 2023

SUPER SHEATH

FDA Adverse Event
Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 12, 2019