6,860 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LASSY LEGS
FDA Adverse Event
Injury
·TEE VEE BRANDS INT'L LTD.·Product code KCX·January 17, 2012
TE SYSTEM
FDA Adverse Event
AMERICAN HAIR REMOVAL SYSTEM·Product code KCX·August 14, 1996
VERSEO EGLIDE
FDA Adverse Event
Malfunction
·VERSEO·Product code KCX·October 2, 2014
VECTOR
FDA Adverse Event
Other
·VECTOR·Product code KCX·December 31, 2003
IGIA FINALLY GONE HAIR REMOVAL SYSTEM
FDA Adverse Event
Injury
·TACTICA INTERNATIONAL·Product code KCX·February 2, 2005
VERSEO EPEN
FDA Adverse Event
SHARPER IMAGE·Product code KCX·January 21, 2012
Epilator, High Frequency, Tweezer-Type
FDA classification
FDA Class 1
·Epilator, High Frequency, Tweezer-Type
DCX
FDA UDI
OSKO, INC.·00869126000468·Stationary X-Ray System
KCI Manufacturing
FDA registration
KCI Manufacturing·3 products·🇮🇪 Ireland
GCX Corporation
FDA registration
GCX Corporation·3 products·🇺🇸 United States
GCX CORPORATION
FDA registration
GCX CORPORATION·1 product·🇺🇸 United States
KCI USA, INC.
FDA registration
KCI USA, INC.·3 products·🇺🇸 United States
KCI USA, INC.
FDA registration
KCI USA, INC.·3 products·🇺🇸 United States
KCL MANUFACTURING, LLC
FDA registration
KCL MANUFACTURING, LLC·1 product·🇺🇸 United States
KCI POLYMEDICS BV
FDA registration
KCI POLYMEDICS BV·1 product·🇧🇪 Belgium
COLLEAGUE (3CX, 3, CX) VOLUMETRIC INFUSION PUMP
FDA 510(k)
FDA Class 2
·General Hospital
GRAFTCAGE ACX
FDA 510(k)
FDA Class 2
·Orthopedic
CAPIOX RX25 OXYGENATOR EAST
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·October 6, 2016
Calibrate CCX Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
COMPUTER CONTROLLED EXTENSION (CCX)
FDA 510(k)
FDA Class 2
·Radiology