12 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Vonflex S Putty
FDA 510(k)
FDA Class 2
·Dental
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169524293·TRIAL 2152518 MEDIUM 12 DEGREES 18MM
LEONE SPA
FDA UDI
LEONE SPA·08033707014362·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 18
INNESIS PEEK CERVICAL CAGE
FDA UDI
BK MEDITECH CO.,LTD.·08809763504747·Distraction Screw
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161121525180·Trial Liner 20° 28/48-50 (B)
DS2ADV AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·April 20, 2024
PIEZOSURGERY
FDA 510(k)
FDA Class 2
·Dental
SYNSTER (CERVICAL,ALIF, PLIF, PTLIF AND TLIF) CAGE HERA CERVICAL CAGE RHEA PLIF CAGE TALON TIFA CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 13, 2025
IAB: 7.5 FR - 40 CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·October 6, 2014
MIRADRY SYSTEM
FDA Adverse Event
Injury
·MIRAMAR LABS INC.·Product code OUB·June 4, 2013
HUDSON OPTI-NEB COMPRESSOR
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAF·June 21, 2011