13 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SImmetry Sacroiliac Joint Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
Orthopedic Salvage System (OSS)
FDA UDI
Biomet Orthopedics, LLC·00880304674417·
Apex Connect
FDA UDI
META SYSTEMS CO., LTD.·08809455601976·Apex Connect Main Body
4CIS VANE SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BEAUTIFIL FLOW
FDA 510(k)
FDA Class 2
·Dental
CAPTURED HIP SCREW 135 DEGREE 4 HOLE PLATE
FDA Adverse Event
Malfunction
·BIOMET TRAUMA·Product code KTT·May 3, 2017
CAPTURED HIP SCREW LAG SCREW
FDA Adverse Event
Malfunction
·BIOMET TRAUMA·Product code KTT·May 3, 2017
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·July 6, 2011
ANGIODYNAMICS
FDA Adverse Event
Injury
·ANGIODYNAMICS·Product code LJT·June 3, 2013
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 10, 2008
VERSA-FXII SC TUBE PLT 90DX16H, 95DX16H, 95DX18H, 95DX20H, 95DX22H
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 21, 2017
TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
FDA Recall
Terminated
·Theralase Inc.·Product code NHN·September 26, 2019
TLC-2000 Therapeutic Medical Laser System, Power Pack component TLC-2002 Used for the temporary relief of knee pain.
FDA Recall
Terminated
·Theralase Inc.·Product code NHN·September 26, 2019