Medical Device Manufacturer · KR , Anyang-Si

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

7 submissions · 7 cleared · Since 2023
7
Total
7
Cleared
0
Denied

Ossvis Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Anyang-Si, KR.

Latest FDA clearance: Dec 2024. Active since 2023. Primary specialty: Dental.

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

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

FDA 510(k) Regulatory Record - Ossvis Co., Ltd.
7 devices
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