8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ORCEPAD
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GC Initial™
FDA UDI
Gc America Inc.·J0228751231·GC Initial™ Zr-FS Cervical Transluc. CT-23, 20g
GC Initial™
FDA UDI
Gc America Inc.·15400556707217·GC Initial™ Zr-FS Cervical Transluc. CT-23, 20g
SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
KMW HIP PROSTHESIS POROUS COATED
FDA 510(k)VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·June 16, 2014
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 19, 2010
TM COLLARLESS FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LPH·December 12, 2012