Medical Device Manufacturer · US , San Clemente , CA

Lightmed USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Lightmed USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Clemente, US.

Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Radiology.

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

Lightmed USA, 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 - Lightmed USA, Inc.

2 devices

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