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

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IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB

FDA 510(k)
FDA Class 2 ·Immunology

Advance Dental Products

FDA UDI
The Atlanta Dental Supply Company·10850455007218·Advance Temporary Crown & Bridge Material A1 Ca...

Denar Slidematic Facebow

FDA UDI
WHIP-MIX CORPORATION·D04020001211·A facebow is a device intended for use in a den...

e-vive NMES System

FDA UDI
Motive Health, Inc.·00854691008124·e-vive NMES System; Extra Small, Right

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167700001210·

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375230867·CERVICAL 1 LEVEL TEMPLATE L21

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375232250·ANTERIOR CERVICAL PLATE, 1 LEVEL L21

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S1700001210·

RX VIATRAC 14 PERIPHERAL DILATATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

AESCULAP BONE WAX

FDA 510(k)
FDA Unclassified ·Unknown

EZ-28 DELIVERY SYSTEM

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code MSS·December 17, 2010

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·January 9, 2025

VIS PÉDICULAIRE POLYAXIALE Ø5,5 LG50

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code NKB·April 28, 2016

VIS PÉDICULAIRE POLYAXIALE Ø5,5 LG40

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code NKB·April 28, 2016

NEURON DELIVERY CATHETER 070

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DQY·January 13, 2011

PROCLAIM 7 ELITE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 16, 2018

SWIFT-LOCK ANCHOR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 16, 2018

SWIFT-LOCK ANCHOR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 16, 2018

OCTRODE LEAD KIT, 60CM LENGTH

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code GZB·January 16, 2018

VASCUTRAK 2 PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·February 8, 2013