Medical Device Manufacturer · CN , Anyang-Si, Gyeonggi-Do

PDX Co., Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026
1
Total
1
Cleared
0
Denied

PDX Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Anyang-Si, Gyeonggi-Do, CN.

Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by PDX Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Strong Systems, Inc. as regulatory consultant.

PDX Co., Ltd. — FDA 510(k) Products and Clearance History

1 devices
1-1 of 1
Filters
All1 Radiology 1