Genoray Co., Ltd.
Genoray Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2026.
Top product codes for Genoray Co., Ltd.
Recent clearances by Genoray Co., Ltd.
- K252229 — BELLIGER ACE
- K250060 — GT300; GT300-C
- K243420 — HESTIA
- K232085 — DVAS (DVAS-M, DVAS-W)
- K232158 — GenX-CR
- K230787 — Oscar 15 & Oscar 15i
- K220392 — PAPAYA 3D & PAPAYA 3D Plus
- K220423 — PAPAYA & PAPAYA Plus
- K211780 — ZEN-2090 Turbo
- K200469 — PAPAYA 3D Premium & PAPAYA 3D Premium Plus
- K181943 — OSCAR (OSCAR Prime, OSCAR Classic)
- K172810 — PORT-X IV
- K172180 — OSCAR 15
- K150354 — PAPAYA 3D Plus
- K140041 — ZEN-7000,SYSTEM,FLUROSCOPIC X-RAY SYSTEM
- K141700 — PAPAYA PLUS, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
- K130419 — PAPAYA PLUS, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
- K130088 — PORT VIEW, DIGITAL X-RAY SENSOR SYSTEM
- K120263 — VOLUX 21C, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
- K103181 — ZENIS, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM
- K103182 — TRIANA, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM
- K092171 — VOLUX, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
- K091918 — ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO
- K063121 — PORTABLE X-RAY SYSTEM, MODEL PORT-X II
Data sourced from openFDA. This site is unofficial and independent of the FDA.