8 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
OMNIFIT (TM) TOTAL KNEE PROSTHESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ROC LUMBAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SUITESTENSA
FDA 510(k)
FDA Class 2
·Radiology
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·September 3, 2020
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 10, 2014
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·October 11, 2010
INTEGRATED APD SET W/CASSETTE3 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 10, 2012
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·April 9, 2018