Medical Device Manufacturer · US , Houston , TX

Curae'Lase, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Curae'Lase, Inc. has 2 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 2 cleared submissions from 2005 to 2014. Primary specialty: Physical Medicine.

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

Curae'Lase, Inc. is one of 18972 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Curae'Lase, Inc.

2 devices

1-2 of 2