10 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EnsoSleep
FDA 510(k)
FDA Class 2
·Neurology
BI-METRIC HIP SYSTEM
FDA UDI
Biomet Uk Ltd·00880304253032·
LASER HAIR GROWTH CAP
FDA Adverse Event
Injury
·UNKNOWN·Product code OAP·February 26, 2025
INNERCHANGE MICRO-INTRODUCER CATHETER, MODELS 7900 THROUGH 7905
FDA 510(k)
FDA Class 2
·Cardiovascular
MILLENIUM ANTI-SNORING DEVICE
FDA 510(k)
FDA Class 2
·Dental
PENUMA IMPLANT
FDA Adverse Event
Injury
·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019
CAPSUREFIX
FDA Adverse Event
Injury
·MPRI·Product code DTB·October 10, 2014
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 14, 2011
VERSAFITCUP CC TRIO ACETABULAR SHELL 56
FDA Adverse Event
MEDACTA INTERNATIONAL SA·Product code KWA·June 5, 2013
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/10MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·December 5, 2018