11 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EPIQ Diagnostic Ultrasound System, EPIQ 5 Diagnostic Ultrasound System, EPIQ 7 Diagnostic Ultrasound System, Affiniti 30 Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583030074·ENCHANT 60 MNR T FW 1.0
MUSTMINI OCCIPITAL SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025
AHWON'S IPL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RENEGADE WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 17, 2014
6000CMS
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 11, 2013
LH SLIDE STAINER
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code GIF·July 28, 2011
Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
FDA Enforcement
Class II
·Terminated·Integra LifeSciences Corp.·April 24, 2019
MUSTMINI OCCIPITAL SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025
MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024