16 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOL PORTABLE DIODE LASER UNIT (WITH WIRELESS FOOT CONTROL)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWP·March 31, 2016
VTS1000
FDA 510(k)
FDA Class 1
·General Hospital
MPS (OR MPS-T)
FDA 510(k)
FDA Class 2
·Neurology
AP409 -PRIMARY INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·December 18, 2025
AP205 - INFUSION SET WITH NON-VENTED SPIKE, 1.2UM FILTER AND NEEDLE Y-SITE
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 5, 2024
AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 6, 2024
AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 17, 2024
AP403 - MICROBORE INFUSION SET WITH VENTED/NON-VENTED SPIKE
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·March 31, 2026
1.6MM X 14MM FULL THREADED SCREW, LOCKING
FDA Adverse Event
Malfunction
·OSTEOMED, LLC·Product code HWC·March 31, 2021
1.6MM, 3 X 8 HOLES, "Y" PLATE
FDA Adverse Event
Malfunction
·OSTEOMED, LLC·Product code HRS·March 31, 2021
1.6MM X 16MM FULL THREADED SCREW, LOCKING
FDA Adverse Event
Malfunction
·OSTEOMED, LLC·Product code HWC·March 31, 2021
AP407 - INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER AND NEEDLELESS Y-SITE
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·March 4, 2026
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 4, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011