10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DYONICS PLAN HIP IMPINGEMENT PLANNING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Derf Needle Holder
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896122673·Derf Needle Holder Mini Tungsten Carbide Dust Tip
ZENITH PEDICLE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PLAYTEX UNSCENTED CARDBOARD APPLICATOR TAMPON #13203 (COLORED) AND # 13203 PV (NON-COLORED)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
STEM: AMISTEM H HA COATED STD STEM SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 13, 2020
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 29, 2025
ALYTE Y-MESH GRAFT
FDA Adverse Event
Injury
·BARD SHANNON LIMITED -3005636544·Product code OTO·May 16, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·June 17, 2011
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·August 22, 2008
PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
FDA Adverse Event
Injury
·PALL NEWQUAY·Product code CAH·May 21, 2014