16 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Venture
FDA UDI
TIDI PRODUCTS, LLC·00618125114146·Nonwoven Sponges, Closed Weave, 4 Ply, 2" x 2"
TWINFIX
FDA UDI
Stryker GmbH·04546540211019·Rack for 2 Implant Modules
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0120220·Assembly, Screwdriver, Extended Tab
DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
DiaTemp Flow
FDA 510(k)
FDA Class 2
·Dental
PRIMING SET FOR ARTERIAL BLOODLINES
FDA Adverse Event
Malfunction
·REYNOSA MANFACTURING·Product code KOC·May 13, 2014
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
LERADO GLOBAL·Product code ILS·January 11, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 1, 2010
SENSIA IPG
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·August 10, 2022
MEDTRONIC LEAD
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DXY·August 10, 2022
APOLLO
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 27, 2023
SYRINGE 10ML 21G 1-1/4IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·February 26, 2020
PROTECTA VR
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LWS·August 10, 2022
ENSURA DR MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·August 10, 2022
PROTECTA XT DR
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LWS·August 10, 2022