9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSALE SEMI-AUTOMATIC BIOPDY INSTRUMENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091982085·posteriors; shade C2; size M; lower jaw
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471118805·K-WIRE - DOUBLE TROCAR 0.8mm DIA x 125mm
CAPILLARYS IMMUNOTYPING, MODEL 2100
FDA 510(k)
FDA Class 2
·Immunology
Balanced Knee Revision System Trabecular Tibial Cone Augments
FDA 510(k)
FDA Class 2
·Orthopedic
COOK SPECTRUM
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·January 21, 2020
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 8, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·February 8, 2011
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·August 5, 2014