8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BEECH PROLOK
FDA 510(k)
FDA Class 2
·General Hospital
Ventura NanoMetalene System
FDA UDI
Seaspine Orthopedics Corporation·10889981151881·Ventura NM Trial, 9mm x 24mm x 15mm, Lordotic
MEDTRADE PRODUCTS ANTISEPTIC BARRIER SILVER FOAM DRESSING, MODEL 09912450
FDA 510(k)
FDA Unclassified
·Unknown
CoolSculpting Elite System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AXIOM ARISTOS VX PLUS
FDA Adverse Event
Injury
·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD·Product code MQB·April 7, 2021
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 29, 2013
ENSEAL TRIO 3MM CURVE TIP 35 C
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·December 21, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 15, 2014