19 results · 23ms · Sources: EU EUDAMED, US FDA

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STERNIC IMPLANT 4.2MM RN, 1.8MM, 8.0MM / 4.1MM RN, 1.8MM, 10.MM / 4.1 MM RN, 1.8MM, 12.0MM / 4.1MM RN, 1.8MM, 14.0MM ...

FDA 510(k)
FDA Class 2 ·Dental

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776186371·MAYO SCISSORS . STRAIGHT DELICATE

SPI VARIOMULTI ANGLED ABUTMENT

FDA 510(k)
FDA Class 2 ·Dental

CORERESTORE 2

FDA 510(k)
FDA Class 2 ·Dental

VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·January 15, 2026

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code DXY·February 9, 2013

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code DXY·February 9, 2013

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code DXY·February 9, 2013

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Death ·RICE CREEK MFG·Product code DXY·December 4, 2012

2520274-2013-02536

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·May 14, 2013

PSI SD800.421 PEEK IMPLANT

FDA Adverse Event
Injury ·SYNTHES MEZZOVICO·Product code GXN·September 23, 2014

PAIN CARE 3000

FDA Adverse Event
Injury ·BREG, INC.·Product code FRN·May 25, 2011

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Death ·RICE CREEK MFG·Product code DXY·December 4, 2012

VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 25, 2023

VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·June 1, 2023

VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 9, 2023

VIDEO TELESCOPE "ENDOEYE HD II", 10 MM, 30°, AUTOCLAVABLE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·April 5, 2023

Y-KNOT FLEX 1.3MM ALL-SUTURE ANCHOR WITH ONE NO. 2 WHITE/BLUE HI-FI SUTURE

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code MBI·April 23, 2019

INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021