532 results · 24ms · Sources: EU EUDAMED, 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