14 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Venus Legacy Pro Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Life Instruments
FDA UDI
Life Instrument Corporation·M930719152830·Teardrop Curette 8mm Lateral Angle
Life Instruments
FDA UDI
Life Instrument Corporation·M930719152800·Teardrop Curette 8mm
NONE
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009
3M COMPLY LEAD FREE PROCESS INDICATORS FOR STEAM
FDA 510(k)
FDA Class 2
·General Hospital
PIONEER ASPECT ANTERIOR CERVICAL PLATE MODEL 24-SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915283S10·15" Teardrop Curette 8mm, Lat ang right 35°, 7"...
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915281S10·15" Teardrop Curette 8mm, 15° fwd ang, 7" handle
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915284S10·15" Teardrop Curette 8mm, Lat ang left 35°, 7" ...
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 2, 2024
TENOR SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009
CHISEL-FLAT-STRAIGHT W/8
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZO·June 26, 2013
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011
ACCU-CHEK COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·September 26, 2008