26 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ELECTRODE NEEDLES
FDA 510(k)
FDA Class 2
·Physical Medicine
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169056046·CAM SPREADER TRIAL 3990015 0 DEG 15MM
ReLine
FDA UDI
Nuvasive, Inc.·00195377080349·RELINE C Handle, Torque 26in-lbs
NA
FDA UDI
Richard Wolf GmbH·04055207045053·AMNIOSCOPE TUBE ID 9.4MM OD 12MM for adults, T...
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000703820·CAM SPREADER TRIAL 3990015 0 DEG 15MM
VENTRALIGHT
FDA UDI
Davol Inc.·00801741130991·Ventralight ST Mesh with Echo 2 Positioning Sys...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189794·AK3 Femoral Sizer
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981172442·IMPLANT TRIAL, TOP LOADING, 10MM
Pro-Retractor Segmented Ring
FDA UDI
KOROS U.S.A., INC.·10840199542205·Pro-Retractor Segmented Ring Medium 10-1/2 x 15"
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·INTERGEL ADHESION PREVENTION SOLUTION
Ballancer Gold, 1212
FDA 510(k)
FDA Class 2
·Physical Medicine
SERUM, CREATININE PHOSPHOKINASE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·GYNECARE INTERGEL ADHESION PREVENTION SOLUTION
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·GYNECARE INTERGEL ADHESION PREVENTION SOLUTION
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024564022·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024564039·
NEXGEN LPS-FLEX ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 17, 2017
NEXGEN LPS PRECOAT FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NJL·June 15, 2016
CONTOUR LINK
FDA Adverse Event
Injury
·BAYER HEALTHCARE LLC·Product code NBW·March 5, 2013
PORTEX D.I.C. TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS NEPHEW ASD INC·Product code JOH·February 9, 2011