Medical Device Manufacturer · US , Oviedo , FL

Sheaumann Laser, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

Sheaumann Laser, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oviedo, US.

Historical record: 2 cleared submissions from 2012 to 2015. Primary specialty: General & Plastic Surgery.

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

Sheaumann Laser, Inc. is one of 4874 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sheaumann Laser, Inc.

2 devices

1-2 of 2