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

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COR18001613-000

FDA Adverse Event
No answer provided ·Product code GEX·October 9, 2018

COR18001925-000

FDA Adverse Event
No answer provided ·Product code GEX·December 21, 2018

COR25000418-000

FDA Adverse Event
No answer provided ·Product code GEX·October 29, 2025

COR18001735-000

FDA Adverse Event
No answer provided ·Product code GEX·November 13, 2018

COR18001736-000

FDA Adverse Event
No answer provided ·Product code GEX·November 13, 2018

COR25000310-000

FDA Adverse Event
No answer provided ·Product code GEX·July 31, 2025

COR20000149-000

FDA Adverse Event
No answer provided ·Product code GEX·June 22, 2020

COR20000124-000

FDA Adverse Event
No answer provided ·Product code GEX·May 22, 2020

COR24000107-000

FDA Adverse Event
No answer provided ·Product code GEX·June 11, 2024

COR20000148-000

FDA Adverse Event
No answer provided ·Product code GEX·June 22, 2020

COR24000031-000

FDA Adverse Event
No answer provided ·Product code GEX·February 22, 2024

COR24000010-000

FDA Adverse Event
No answer provided ·Product code GEX·January 10, 2024

COR24000011-000

FDA Adverse Event
No answer provided ·Product code GEX·January 10, 2024

COR26000101-000

FDA Adverse Event
No answer provided ·Product code GEX·April 27, 2026

COR26000109-000

FDA Adverse Event
No answer provided ·Product code GEX·April 30, 2026

COR24000344-000

FDA Adverse Event
No answer provided ·Product code GEX·December 18, 2024

COR24000290-000

FDA Adverse Event
No answer provided ·Product code GEX·November 5, 2024

COR16000378-000

FDA Adverse Event
No answer provided ·Product code GEX·August 10, 2016

COR16000374-000

FDA Adverse Event
No answer provided ·Product code GEX·August 9, 2016

COR16000480-000

FDA Adverse Event
No answer provided ·Product code GEX·September 13, 2016