127 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·TORAY SOFT CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·TORAY SOFT CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·TORAY SOFT CONTACT LENSES
Two Striper
FDA UDI
ABRASIVE TECHNOLOGY, INC.·B868C8400441·Abrasive Point
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127021008·Quick Connect Cup Trial Size 44
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
SDI PREPAX DILUKIT 29-1000
FDA 510(k)
FDA Class 1
·Clinical Chemistry
NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MATRIX VASCULAR CLOSURE SYSTEM (VSG)
Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation
FDA Pre-Market Approval
FDA Class 3
·Globe® Pulsed Field System
SYSLOC MINI AVF 15G X 1" BE 30CM /CLAMP
FDA Adverse Event
Injury
·JMS SINGAPORE PTE LTD·Product code FIE·May 30, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·November 20, 2012
LEAD MODEL UNK
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·September 15, 2010
SULOX HEAD, M, A, 28/0, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 8, 2017
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MynxGrip Vascular Closure Device, Mynx Control Vascular Closure Device (VCD)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MynxGrip Vascular Closure Device and two components of Mynx Control Vascular Closure Device (VCD)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE