Medical Device Manufacturer · KR , Ansan-Si

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

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Jaintek Co.,Ltd has 1 FDA 510(k) cleared medical devices. Based in Ansan-Si, KR.

Last cleared in 2022. Active since 2022. Primary specialty: Dental.

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

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Jaintek Co.,Ltd
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