30 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Braces on Demand Bracket
FDA 510(k)
FDA Class 2
·Dental
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG
Conventional Lead Apron .5mm Large 24 X 42
FDA UDI
Flow X Ray Corporation·00843696123550·Conventional Lead Apron .5mm Large 24 X 42, Shi...
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3
MICOR ANESTHESIA CONDUCTION KIT
FDA 510(k)
FDA Class 2
·Anesthesiology
EQUASHIELD SYSTEM PROTECTIVE PLUS
FDA 510(k)
FDA Class 2
·General Hospital
LOTUS VALVE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NPT·April 30, 2020
DESARA
FDA Adverse Event
Injury
·CALDERA MEDICAL, INC.·Product code OTN·October 20, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 27, 2013
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·August 11, 2011
ALINITY C PROCESSING MODULE
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code JJE·September 19, 2019
RESOLUTE ONYX RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·November 6, 2019
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·November 6, 2019
ECHELON ENDOPATH STAPLER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 23, 2024
BLAKE DRAIN UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GBX·July 25, 2024
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·May 26, 2023
CHAIT PERCUTANEOUS CECOSTOMY CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KNT·June 9, 2025
PIPELINE FLEX W/SHIELD TECHNOLOGY
FDA Adverse Event
Malfunction
·MEDTRONIC EUROPE SARL·Product code OUT·February 6, 2022
HANDPIECE MICS
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·October 10, 2019