9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
AQUA DENT HANDPIECE EXTENSION AND AQUA DENT DISP.
FDA 510(k)
FDA Class 1
·Dental
Modulus
FDA UDI
Nuvasive, Inc.·00887517023568·Modulus ALIF Trial, 10x34x28mm 25°SmDeep
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776360917·Silver Dermatome Knife
SHOWCASE
FDA 510(k)
FDA Class 2
·Radiology
TESTOSTERONE RADIOIMMUNOASSY KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 18, 2014
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·October 25, 2010
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·November 12, 2012
EV3 Pipeline Flex Embolization Device with Flex Shield Technology
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021