16 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LOFRIC PRIMO, LOFRIC HYDRO-KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ArgenZ HT+ 98x22 B1
FDA UDI
ARGEN CORPORATION, THE·D818122078·Dental porcelain/ceramic restoration kit
SOLA, COUNTER-PULSATION, MODEL SECP-S
FDA 510(k)
FDA Class 2
·Cardiovascular
RADIOLOGICAL IMAGE PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
2122870-2016-00024
FDA Adverse Event
Malfunction
·January 11, 2016
2122870-2016-00023
FDA Adverse Event
Malfunction
·January 11, 2016
SCREW, UNKNOWN TYPE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019
SCREW, UNKNOWN TYPE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 21, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 19, 2014
PFCSIG POSTLIP INSERT SZ4 10MM
FDA Adverse Event
Injury
·DEPUY-CORK, A DIV. OF DEPUY ORTHOPAEDICS·Product code JWH·June 3, 2011
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·December 18, 2012