Medical Device Manufacturer · US , Santa Monica , CA

Pureway Compliance, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2015

Total

Cleared

Denied

Pureway Compliance, Inc. has 3 FDA 510(k) cleared medical devices. Based in Santa Monica, US.

Latest FDA clearance: Oct 2025. Active since 2015. Primary specialty: General Hospital.

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

Pureway Compliance, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pureway Compliance, Inc.

3 devices

1-3 of 3