Medical Device Manufacturer · US , Peterborough , NH

Soclean, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2024
2
Total
1
Cleared
1
Denied

Soclean, Inc. has 1 FDA 510(k) cleared medical devices. Based in Peterborough, US.

Latest FDA clearance: Oct 2025. Active since 2024. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Soclean, Inc.
2 devices
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