Rayence Co., Ltd. - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Rayence Co., Ltd. has 38 FDA 510(k) cleared radiology devices. Based in Houston, US.
Latest FDA clearance: Mar 2025. Active since 2011.
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 Rayence Co., Ltd.
38 devices
Cleared
Mar 12, 2025
2430TCA with Xmaru W
Radiology
86d
Cleared
Sep 09, 2024
Digital Flat Panel X-ray Detector (1717WCE, 1717WCE-HR, 1717WCE-HS, 1717WCE-GF)
Radiology
27d
Cleared
Mar 07, 2024
0909FCC, 0909FCC-HS
Radiology
29d
Cleared
Jun 21, 2023
1417WCE, 1417WCE-HR, 1417WCE-HS, 1417WCE-GF
Radiology
30d
Cleared
May 06, 2022
Vatech Clismile
Dental
58d
Cleared
Oct 18, 2021
0909FCB, 1212FCA
Radiology
48d
Cleared
Jun 21, 2021
2430MCA with Xmaru W
Radiology
265d
Cleared
Apr 28, 2021
1717FCC
Radiology
27d
Cleared
Oct 26, 2020
1212FCA
Radiology
39d
Cleared
Jul 23, 2020
1717SCV, 1717SGV
Radiology
23d
Cleared
Apr 30, 2019
XmaruView V1 (Xmaru Chiroview, Xmaru Podview)
Radiology
27d
Cleared
Mar 01, 2019
ClearON Mobile
Radiology
74d
Looking for a specific device from Rayence Co., Ltd.? Search by device name or K-number.
Search all Rayence Co., Ltd. devices