532 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMA 3D
FDA UDI
EMA SLEEP INCORPORATED·00850077473791·An intra oral appliance intended for mandibular...
KAVA DORSAL ACRYLIC
FDA UDI
APEX DENTAL SLEEP LAB INCORPORATED·00860008847508·A dental acrylic oral appliance intended for ma...
KAVA HERBST DUAL LAMINATE
FDA UDI
APEX DENTAL SLEEP LAB INCORPORATED·00860008847539·A Dental Dual laminate oral appliance intended ...
KAVA DORSAL DUAL LAMINATE
FDA UDI
APEX DENTAL SLEEP LAB INCORPORATED·00860008847522·A Dental Dual-Laminate oral appliance intended ...
KAVA HERBST ACRYLIC
FDA UDI
APEX DENTAL SLEEP LAB INCORPORATED·00860008847515·A custom acrylic oral appliance intended to sup...
QUICKIE 2 WHEELCHAIR
FDA Adverse Event
Malfunction
·QUICKIE DESIGNS INC.·Product code IOR·November 19, 1996
NTI TENSION SUPPRESSION SYSTEM
FDA Adverse Event
Injury
·NTI·Product code LQZ·March 2, 2010
MMRNA
FDA Adverse Event
Injury
·VIVOS THERAPEUTICS INC.·Product code LQZ·November 23, 2021
NTI SPLINT
FDA Adverse Event
Injury
·NTI CLENCHING SUPPRESSION SYSTEM·Product code LQZ·July 3, 2003
NTI-TSS DENTAL DEVICE
FDA Adverse Event
Injury
·KELLER LABS·Product code LQZ·September 9, 2004
NARVAL CC ORTHESE MRD
FDA Adverse Event
Injury
·RESMED SAS·Product code LQZ·July 30, 2014
NARVAL CC ORTHESE MRD
FDA Adverse Event
Injury
·RESMED SAS·Product code LQZ·July 30, 2014
NTI REFILL KIT-NIGHTLINE
FDA Adverse Event
Other
·HERAEUS KULZER, INC.·Product code LQZ·March 14, 2000
REFILL NTI KIT
FDA Adverse Event
Injury
·HERAEUS KULZER, INC.·Product code LQZ·January 10, 2000
NARVAL CC ORTHESE MRD
FDA Adverse Event
Other
·RESMED SAS - DENTAL SLEEP BUSINESS·Product code LQZ·October 31, 2012
NTI REFILL KIT - NIGHTTIME
FDA Adverse Event
Injury
·HERAEUS KULZER, INC.·Product code LQZ·November 23, 1999
NTI-TSS
FDA Adverse Event
Injury
·NTI-TSS·Product code LQZ·October 1, 2004
NTI
FDA Adverse Event
Injury
·NTI·Product code LQZ·February 4, 2009
NTI TENSION SUPPRESSION SYSTEM
FDA Adverse Event
Injury
·THERAPEUTIC SOLUTIONS INTERNATIONAL·Product code LQZ·February 11, 2016
NOT APPLICABLE
FDA Adverse Event
Injury
·Product code LQZ·July 17, 2012