Genoray Co., Ltd. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Genoray Co., Ltd. has 23 FDA 510(k) cleared radiology devices. Based in Flintville, US.
Latest FDA clearance: Oct 2025. Active since 2007.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Genoray Co., Ltd.
23 devices
Cleared
Oct 08, 2025
GT300
Radiology
271d
Cleared
Jul 17, 2025
HESTIA
Radiology
255d
Cleared
Dec 08, 2023
DVAS (DVAS-M, DVAS-W)
Radiology
148d
Cleared
Sep 13, 2023
GenX-CR
Radiology
55d
Cleared
Jul 20, 2023
Oscar 15 & Oscar 15i
Radiology
120d
Cleared
May 19, 2022
PAPAYA 3D & PAPAYA 3D Plus
Radiology
97d
Cleared
May 19, 2022
PAPAYA & PAPAYA Plus
Radiology
94d
Cleared
Mar 09, 2022
ZEN-2090 Turbo
Radiology
273d
Cleared
Sep 16, 2020
PAPAYA 3D Premium & PAPAYA 3D Premium Plus
Radiology
203d
Cleared
Aug 17, 2018
OSCAR (OSCAR Prime, OSCAR Classic)
Radiology
28d
Cleared
Mar 07, 2018
PORT-X IV
Radiology
170d
Cleared
Feb 09, 2018
OSCAR 15
Radiology
205d