862 results
·
21ms
·
Sources: EU EUDAMED, US FDA
NXSTAGE DOSING CALCULATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169604872·SPACER 2130460 OLIF25 27MM 0 DEG 14X60
Biogel
FDA UDI
Bosma Enterprises·10818634023343·Biogel Surgeons 6.0 - 50 Pair/Box
FeetSupport™, rotatable 2.0
FDA UDI
MACROMEDICS B.V.·08720168160263·FeetSupport, rotatable 2.0
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981176150·Z-Rod, Dia. 6.0mm, Titanium, 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529583255·Apex Femoral Nail PF Left Ø 13.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529588458·Apex Femoral Nail Retrograde Ø 13.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587482·Apex Femoral Nail GT Right Ø 13.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585686·Apex Femoral Nail PF Right Ø 13.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586584·Apex Femoral Nail GT Left Ø 13.0 x 460mm
MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SMARTLUX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UniSyn® Hip System
FDA UDI
CONSENSUS ORTHOPEDICS, INC.·00844588012280·Neck, Standard, Cementless
UniSyn Hip System
FDA UDI
Shalby Advanced Technologies, Inc.·00840286836500·Neck, Standard, Cementless, 30mm, 46mm
LIKORALL
FDA Adverse Event
Malfunction
·LIKO AB·Product code FSA·March 26, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 16, 2011
OSTY-CUT BONE BIOPSY NEEDLE
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code KNW·August 20, 2008
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026