11 results
·
21ms
·
Sources: EU EUDAMED, US FDA
PACEPAC
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209113217·
INEX Absorbable Nasal Implant
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
COLOR NIO 2MP, E-2320 C
FDA 510(k)
FDA Class 2
·Radiology
ACUSNARE POLYPECTOMY SNARE
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KNS·May 10, 2022
FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM
FDA Adverse Event
Malfunction
·FLEXIBLE STENTING SOLUTIONS·Product code FGE·June 6, 2014
1020279-2012-00646
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·November 30, 2012
1-DAY ACUVUE
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON VISION CARE, INC.·Product code LPL·September 29, 2010
ACUSNARE POLYPECTOMY SNARE SOFT
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KNS·July 13, 2023
ACUSNARE POLYPECTOMY SNARE
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KNS·May 4, 2022
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026