92 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUATTRO GL SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517636973·CoRoent Ant TLIF PEEK, 13x11x32mm 15°
Dukal
FDA UDI
Dukal LLC·00665973002835·Gauze Pad 3" x 3" 12-Ply, Sterile
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321313250·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311313250·
EVOLUTION MP ADAPTIVE CS INSERT
FDA 510(k)
FDA Class 2
·Orthopedic
STELLARIS PC VISION ENHANCEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
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
STELLARIS VISION ENHANCEMENT SYSTEM
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQC·February 5, 2026
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
PARIETEX UGYTEX PP ANTERIOR KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTP·May 17, 2013
SONICISION
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code LFL·September 17, 2014
VITA 2
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NVZ·June 16, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NKB·July 12, 2019