8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Scenium
FDA 510(k)
FDA Class 2
·Radiology
BI-METRIC(R) HEAD/NECK PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304307315·
K162309
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019
CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DERMOTHERAP GUN
FDA 510(k)
FDA Class 2
·General Hospital
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 11, 2013
PINN MAR +4 10D 32IDX50OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 7, 2011
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·October 10, 2014