8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
PERCUTANEOUS TRACHEOSTOMY DEVICE
FDA 510(k)
FDA Class 2
·Anesthesiology
NAIL HOLDING SCREW
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·January 6, 2012
DENTAL IMPLANT COPING (PROSTHETIC ACCESSORIES TO THE ITI DENTAL IMPLANT SYSTEM)
FDA 510(k)
FDA Class 2
·Dental
VALVED TEARAWAY INTRODUCER GENERATION II
FDA 510(k)
FDA Class 2
·Cardiovascular
GEMSTR 7 THPY ALT ST
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·March 27, 2014
VENTED AUTOFEED CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 14, 2012
TECNIS CL
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·September 13, 2010
PTFE Wire Guide, Guidewire, Global Product Number 638813 635413-10
FDA Enforcement
Class II
·Terminated·Cook Inc.·February 12, 2020