21 results · 21ms · Sources: EU EUDAMED, US FDA

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Ultra ICE Plus – PI 9 MHz Peripheral Imaging Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Halyard

FDA UDI
Avanos Medical, Inc.·10680651928488·HYH,UBLOCK,UBT,-,-,10

AVANOS

FDA UDI
Avanos Medical, Inc.·00193493928484·AVANOS* Universal Block Trays

Cranial Guidance Software

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327538328·Cranial Guidance Sales Demo

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361038979·Rasp Trial Head, 38X28 Lordotic 8°, 17L

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361038931·Rasp Trial Head, 38X28 Lordotic 8°, 9L

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361038948·Rasp Trial Head, 38X28 Lordotic 8°, 11L

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361038955·Rasp Trial Head, 38X28 Lordotic 8°, 13L

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361038962·Rasp Trial Head, 38X28 Lordotic 8°, 15L

ENDOSKELETON® TA

FDA UDI
TITAN SPINE, LLC·00191375051329·7 Deg Lordotic, Implant Caddy, Base, Large

ENDOSKELETON® TA

FDA UDI
TITAN SPINE, LLC·00191375051336·7 Deg Lordotic, Implant Caddy, Base, X-Large

ENDOSKELETON® TA

FDA UDI
TITAN SPINE, LLC·00191375051305·7 Deg Lordotic, Implant Caddy, Base, Standard

MICROTHERMX-100 MICROWAVE ABLATION SYSTEM AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

BLADEVIEW

FDA 510(k)
FDA Class 2 ·Radiology

OSSURE LOEP KIT

FDA Adverse Event
Death ·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·December 27, 2018

OSSURE LOEP KIT

FDA Adverse Event
Death ·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·January 18, 2020

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 20, 2013

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 1, 2011

HEARTSTRING II PROXIMAL SEAL SYSTEM

FDA Adverse Event
Malfunction ·GUIDANT CARDIAC SURGERY·Product code DXC·September 29, 2008

CHROMID® CARBA SMART

FDA Adverse Event
Malfunction ·BIOMERIEUX S.A.·Product code JSO·August 23, 2018