13 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRAMA White Implant Systems
FDA 510(k)
FDA Class 2
·Dental
Maestro™ Total Wrist
FDA UDI
Biomet Orthopedics, LLC·00887868239854·
MAESTRO TOTAL WRIST
FDA UDI
Biomet Orthopedics, LLC·00880304481091·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197453110·CCR Titanium Lateral Blade
24x65m...
FARRELL VALVE WITH CORFLO ANTI-IV CONNECTORS MODEL 20-4300AIV
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
REAMER SHAFT, MOD. TRINKLE BIXCUT 8.0 X 284 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·December 18, 2012
GORILLA/BABY GORILLA PLATING SYSTEM
FDA Adverse Event
Injury
·PARAGON 28, INC·Product code HRS·September 17, 2020
HUDSON SHER-I-BRONCH ACCESSORY PACK
FDA Adverse Event
Malfunction
·TELEFLEX·Product code BTR·October 15, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013
MO.MA ULTRA
FDA Adverse Event
Injury
·INVATEC SPA·Product code NTE·June 22, 2021
SPIDER FX
FDA Adverse Event
Injury
·COVIDIEN·Product code NTE·June 22, 2021