36 results · 27ms · Sources: EU EUDAMED, US FDA

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LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM

FDA 510(k)
FDA Class 1 ·Ophthalmic

BIOSLING - BIOABSORBABLE POLYMER SLING & SURGICAL MESH

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

VOCOM IMPLANT- 8MM

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

INDIGO SYSTEM ASPIRATION CATHETER 5

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·November 21, 2016

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·December 10, 2020

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·June 5, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·July 28, 2020

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·July 29, 2020

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·September 11, 2020

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·September 24, 2019

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·March 27, 2013

PD1200 DEFIBRILLATOR/PACEMAKER

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code LDD·June 11, 2008

FLOGARD

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·April 18, 2011