22 results · 22ms · Sources: EU EUDAMED, US FDA

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LIFTKAR PT

FDA 510(k)
FDA Class 2 ·Physical Medicine

C-Arc Holder,Adjustable in Height

FDA UDI
Noras MRI products GmbH·04251269203336·

Flexitron

FDA UDI
Nucletron B.V.·08717213026995·Flexitron Transfer Tube for 4F Flexibles (8)

INTERLINK THREADED LOCK CANNULA

FDA 510(k)
FDA Class 2 ·General Hospital

PEDIATRIC HEAD-SPINE COIL (MODEL:5000012701

FDA 510(k)
FDA Class 2 ·Radiology

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

GELB MOUTHGUARD

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·April 10, 2019

ASTRON CLEAR SPRINT

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 14, 2020

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 17, 2019

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 16, 2019

ASTRON CLEAR SPLINT

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 22, 2020

ASTRON CLEAR SPLINT LOWER

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 30, 2020

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·May 4, 2020

GUARDIAN ROLLING WALKER

FDA Adverse Event
Malfunction ·A&E·Product code ITJ·November 4, 2008

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 14, 2013

MIRAGE .008 HYDROPHILIC GUIDEWIRE

FDA Adverse Event
Malfunction ·EV3 NEUROVASCULAR·Product code DQX·August 13, 2008

ASTRON CLEAR SPLINTS

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 2, 2020

BD Interlink threaded lock cannula This is a locking blunt plastic cannula specifically designed for IV connection to an Interlink¿ injection site. It is screwed down over the Interlink¿ injection site and a blunt plastic cannula inside the housing enters the Interlink¿ injection site to provide a pathway for IV fluid administration.

FDA Enforcement
Class II ·Terminated·Becton Dickinson & Company·January 22, 2014