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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DePuy ATTUNE™ Total Knee System

FDA 510(k)
FDA Class 2 ·Orthopedic

AGXO

FDA UDI
Oticon A/S·05707131354549·G300 S, MINIRITE T 312 2.4G C063 AGXO

24PW - Hanta Virus

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013442·Hanta Virus - 24 Poly White

24M - Tampa Electric Co.

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383534376·"An absorbent paper points is an endodontic pap...

HVP CANNULA SET, M-HUB SERIES (6)

FDA UDI
The Wells Johnson Company·B458201347010·Cannula Set, HVP Cannula Set, M-Hub Series (6),...

HVP CANNULA SET, STANDARD (7)

FDA UDI
The Wells Johnson Company·B458201347000·Cannula Set, HVP Cannula Set, Standard (7), con...

MODIFICATION TO M2376A DEVICELINK SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

MERIDIAN-II AND MERDIAN-PLUS

FDA 510(k)
FDA Class 2 ·Neurology

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·August 8, 2018

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·August 8, 2018

ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

FDA Adverse Event
Injury ·COOK, INC.·Product code MIH·March 27, 2014

VASOVIEW HEMOPRO 2

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 20, 2014

DEPUY ASR XL FEM IMP SIZE 43

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 27, 2014

SYNERGY

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 3, 2011

GYNECARE TVT RETROPUBIC SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·July 2, 2013

I-STAT PT/INRCARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code GJS·November 18, 2013

ANEURX

FDA Adverse Event
Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 25, 2014

TALENT AAA

FDA Adverse Event
Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 25, 2014

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MPRI·Product code LWS·December 9, 2013