10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
LDS PEEP VALVE
FDA 510(k)
FDA Class 2
·Anesthesiology
Multiphase Blue ChromiumCobalt
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746050343·WIRE MULTIPHASE BLUE CHROMIUM COBALT LOWER 016X...
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209134465·
Chromium Cobalt Wire
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746203978·WIRE MULTIPHASE BLUE CHROMIUM COBALT LOWER 016X...
CHRONOCOR V EXTERNAL PACER, MODEL 297A
FDA 510(k)
FDA Class 2
·Cardiovascular
MICROINFERTILITY SCISSORS, TITANIUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·June 6, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·December 3, 2012
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021