12 results
·
34ms
·
Sources: EU EUDAMED, US FDA
PARKE-DAVIS AEGIS ABOSRBENT SPONGES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Bioplate®
FDA UDI
Bioplate, Inc.·M3848135950·5-Tab Zip Implant - 16 mm
ARx SAI
FDA UDI
Life Spine, Inc.·00190837189402·
ARx SAI
FDA UDI
Life Spine, Inc.·00190837190873·
ARx SAI
FDA UDI
Life Spine, Inc.·00190837173937·
ARx SAI
FDA UDI
Life Spine, Inc.·00190837173333·
Bioplate®
FDA UDI
Bioplate, Inc.·M384813595US0·5-Tab Zip Implant - 16 mm
PREMIER III PHASED ARRAY CTL SPINE COIL
FDA 510(k)
FDA Class 2
·Radiology
Aqua Medical RF Vapor System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RECAP CEMENT FMRL HD RESUR 52M
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KXA·May 15, 2014
CARELINK PROGRAM W/TELEMETRY C
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DXY·October 31, 2012
RADIAL JAW 3 BIOPSY FORCEPS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·August 25, 2010