9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KARL STORZ CONTACT MICRO-LARYNGOSCOPES
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
V.A.C. ATS LARGE (1000 ML) CANISTER WITH GEL, MODELS M6275093/5, M6275093/10
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAHI Guide Wire Extension
FDA 510(k)
FDA Class 2
·Cardiovascular
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012
G7 HI-WALL E1 LINER 36MM G
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·February 19, 2024
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2014
NEXGEN LPS-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NJL·February 13, 2013
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code MUZ·December 20, 2010
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026