9 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RIGEL 3DR Anterior Cervical Corpectomy System
FDA 510(k)
FDA Class 2
·Orthopedic
RIGIDLOOP
FDA UDI
S.B.M·03760304680182·The RIGIDLOOP device consists of an adjustable ...
EASY-LOAD LENS DELIVERY SYSTEM
FDA 510(k)
FDA Class 1
·Ophthalmic
THERATEARS CONTACT LENS COMFORT DROPS
FDA 510(k)
FDA Class 2
·Ophthalmic
BIOABSORBABLE INTERFERENCE SCREWS
FDA Adverse Event
Malfunction
·S.B.M. SAS·Product code MAI·March 14, 2024
BARD-PARKER
FDA Adverse Event
Malfunction
·ASPEN SURGICAL PRODUCTS, INC.·Product code GES·October 24, 2014
3F AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC ATS, INC.·Product code LWR·August 25, 2011
GYNECARE PROLIFT +M POSTERIOR PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 18, 2013
CARELINK PERSONAL MMT-7333
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code CGA·November 4, 2022