10,000 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNITRAX MODULAR ENDO HEAD 50MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS·Product code KWL·February 5, 2010
NEUROMONICS OASIS TINNITUS DEVICE
FDA Adverse Event
Malfunction
·NEUROMONICS INC·Product code KLW·July 17, 2015
NEUROMONICS OASIS
FDA Adverse Event
Injury
·NEUROMONICS·Product code KLW·May 16, 2010
NEUROMONICS OASIS TINNITUS TREATMENT
FDA Adverse Event
Injury
·NEUROMONICS·Product code KLW·November 6, 2012
NEUROMONICS TINNITUS TREATMENT
FDA Adverse Event
Other
·NEUROMONICS INC.·Product code KLW·August 16, 2007
NEUROMONICS OASIS TINNITUS TREATMENT DEVICE
FDA Adverse Event
Malfunction
·NEUROMONICS INC.·Product code KLW·February 3, 2009
GNRESOUND
FDA Adverse Event
Malfunction
·GNRESOUND·Product code KLW·May 12, 2011
NEUROMONITCS OASIS.
FDA Adverse Event
Injury
·NEUROMONICS, INC.·Product code KLW·February 27, 2015
NEUROMONICS OASIS
FDA Adverse Event
Injury
·NEUROMONICS INC.·Product code KLW·February 20, 2015
PHONAK "HEARING AID MASKERS"
FDA Adverse Event
Injury
·PHONAK·Product code KLW·June 30, 2015
Masker, Tinnitus
FDA classification
FDA Class 2
·Masker, Tinnitus
GLW, Inc.
FDA registration
GLW, Inc.·22 products·🇺🇸 United States
KLC SERVICES, INC./REEP
FDA registration
KLC SERVICES, INC./REEP·1 product·🇺🇸 United States
SHANGHAI ALWINGS MEDICAL INSTRUMENT CO.,LTD.
FDA registration
SHANGHAI ALWINGS MEDICAL INSTRUMENT CO.,LTD.·39 products·🇨🇳 China
76 ELW BITE CHECKER SILICONE
FDA 510(k)
FDA Class 2
·Dental
ACCUWELL TSH, MODEL KAW-TSH-960
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RESUBMITTED CLW ACETABULAR CUP W/SULMESH
FDA 510(k)
FDA Class 2
·Orthopedic
MD Orthopaedics
FDA UDI
MD ORTHOPAEDICS, INC.·00810060883754·AFO SIZE 0 LEFT GRAY
MD Orthopaedics
FDA UDI
MD ORTHOPAEDICS, INC.·00810060884416·AFO SIZE 1 LEFT GRAY
MD Orthopaedics
FDA UDI
MD ORTHOPAEDICS, INC.·00810060885284·AFO SIZE 2 LEFT GRAY