8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP
FDA 510(k)
FDA Class 2
·Orthopedic
Edge™ Diamond PMI014-5F Pear Minimally Invasive
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002875·Diamond dental bur, reusable
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665582393·MIS Cannulated Screw, Ø5.5 x 25mm, Ø5.5mm Rod
MICROLINE SCREEN FOR METHAMPHETAMINE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CYBEX 6000
FDA 510(k)
FDA Class 2
·Physical Medicine
PKG, SLIDING LOCK ATRAUMATIC GRASPER
FDA Adverse Event
Injury
·STRYKER ENDOSCOPY SAN JOSE·Product code KOG·January 9, 2013
KORA
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NVZ·July 7, 2014
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 12, 2009