6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOFTTOUCH II LANCET DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SATURN DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
CYNOSURE PHOTOLIGHT PL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PINNACLE MTL INS NEUT36IDX50OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·January 28, 2013
ENDOPATH** XCEL
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·December 17, 2010
XTRASOFT ORBIT GALAXY DETACHABLE COIL
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code HCG·July 14, 2014