27 results
·
20ms
·
Sources: EU EUDAMED, US FDA
CLEARMEDICAL/NELLCOR OXISENSOR II, NEONATAL/ADULT, MODEL N-25
FDA 510(k)
FDA Class 2
·Cardiovascular
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00126091·
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040133095·Zirlux TR A3 98x18mm
NA
FDA UDI
Smith & Nephew, Inc.·03596010078971·NEEDLE THIMBLE
n/a
FDA UDI
Ortho Development Corporation·00822409072781·Narrow Fully Toothed Broach Size 9
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967187181·Battalion, LLIF Trial, 8°, 26 mm Wide, 09 mm X ...
COLOR SPEX
FDA UDI
FGX INTERNATIONAL INC.·00193033426876·
TINA-QUANT RHEUMATOID FACTORS II TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
ACCUSONIC, MODEL AS-260
FDA 510(k)
FDA Class 2
·Physical Medicine
CAPSTONE SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·May 1, 2018
Octane M
FDA UDI
Choice Spine, LP·10885862236340·
CAPSTONE SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MAX·April 19, 2018
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·March 20, 2013
ASR UNI FEMORAL IMPL SIZE 45
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
LUMOS VR-T
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code LWS·March 10, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code NQP·September 7, 2012
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code NQP·July 6, 2012
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012