85 results · 30ms · Sources: EU EUDAMED, US FDA

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ECLERIS SINUSCOPE

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

CoRoent

FDA UDI
Nuvasive, Inc.·00887517597236·CoRoent Large MP Ti, 13x9x23mm 12°

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131323·TiBase BC WP 1.5G E

DBT, DYNAMIC BUBBLE TRAP

FDA 510(k)
FDA Class 2 ·Cardiovascular

SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS

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

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 14, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·February 22, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

URETEX SUPPORT PP TRANSOBTUR2 KIT X1

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code OTN·May 17, 2013

CARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD.·Product code NVZ·June 16, 2011

THYMATRON

FDA Adverse Event
Malfunction ·SOMATICS, LLC·Product code GWQ·August 6, 2008

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·July 12, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 7, 2017