8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
ROPER-TUKE ELBOW
FDA 510(k)
FDA Class 2
·Orthopedic
FREEDOM HIP SYSTEM CONSTRAINED MODULAR HEAD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·May 31, 2017
LenSx Laser System
FDA 510(k)
FDA Class 2
·Ophthalmic
UNIVERSAL BUCKS TRACTION
FDA 510(k)
FDA Class 1
·Orthopedic
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code KNT·April 17, 2020
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 16, 2014
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·November 14, 2012
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 21, 2010