10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
PANOSOL 2000 624-404
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GC Initial™
FDA UDI
Gc America Inc.·J0228727071·GC Initial™ IQ/Effect Ingot D2-Zr, 5 pcs. X 2g
GC Initial™
FDA UDI
Gc America Inc.·15400556710095·GC Initial™ IQ/Effect Ingot D2-Zr, 5 pcs. X 2g
Arthrex®
FDA UDI
ARTHREX, INC.·00888867386457·Cortical Screw, 2.7 mm x 7 mm
PATIENT CONTOURED MESH-PEEK (PCM-P)
FDA 510(k)
FDA Class 2
·Neurology
Renamel Microfill
FDA 510(k)
FDA Class 2
·Dental
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·June 13, 2014
CENTURY BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·October 8, 2010
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·December 13, 2012
KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE
FDA 510(k)
FDA Class 2
·Neurology