Medical Device Manufacturer · KR , Bucheon-Si

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

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

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

Last cleared in 2023. Active since 2023. Primary specialty: Dental.

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

510(k) submissions have been managed by Provision Consulting Group, Inc. as regulatory consultant.

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