13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
KASHA VISUAL FIELD SYSTEM
FDA 510(k)
FDA Class 1
·Ophthalmic
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902991998·INSTRUMENT 6971156 IMPLANT INSERTER 6MM
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292787·
Sklar
FDA UDI
SKLAR CORPORATION·10649111040047·NAIL NIP DBL SPRG W/LK ANG 5.5
OMNI Anseris Hip Stem
FDA 510(k)
FDA Class 2
·Orthopedic
SOUNMED SD-2000 PLUS PORTABLE ULTRASOUND SCANNER
FDA 510(k)
FDA Class 2
·Radiology
PRESTIGE LP
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code LXH·December 30, 2025
ENDOPATH DILATING TIP TROCAR
FDA Adverse Event
Malfunction
·EES-JUAREZ·Product code GCJ·February 19, 1997
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 1, 2013
*
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT·Product code HBF·January 18, 2011
SEQUOIA AND PATHFINDER NXT CLOSURE TOP
FDA Adverse Event
Injury
·ZIMMER SPINE, INC.·Product code NKB·July 8, 2014
Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017
Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017