Medical Device Manufacturer · KR , Daegu

E.O.S Co., Ltd. - FDA 510(k) Cleared Devices

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

E.O.S Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Daegu, KR.

Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Ophthalmic.

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

510(k) submissions have been managed by Wise Company, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - E.O.S Co., Ltd.
1 devices
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