10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
CollOvine Wound Powder
FDA 510(k)
FDA Unclassified
·Unknown
Minit®
FDA UDI
ZIMMER SPINE, INC.·00889024334243·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690197102·Revision Knee Spiral Reamer- Hudson Short Flute...
Truliant
FDA UDI
Exactech, Inc.·10885862556318·TRIAL, TIBIAL INSERT, CR, NEUTRAL, SIZE 4
Terumo Capiox SX18 Oxygenator/ Hardshell Reservoir, Terumo Capiox SX18 Oxygenator/ Hardshell Reservoir with Xcoating, Terumo Capiox SX25 Oxygenator/Hardshell Reservoir, Terumo Capiox SX25 Oxygenator/Hardshell Reservoir with Xcoating
FDA 510(k)
FDA Class 2
·Cardiovascular
AMBU MARK IV RESUSCITATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 8, 2024
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. /HUNTINGTON·Product code HQL·December 5, 2008
C-FLEX POLAR HEAD POSITIONER
FDA Adverse Event
Other
·ALLEN MEDICAL SYSTEMS·Product code FWZ·August 31, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 29, 2013