Medical Device Manufacturer · KR , Uiwang-Si

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

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

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

Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Dental.

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

510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.

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