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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