Medical Device Manufacturer · US , Forest Hill , TX

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

4 submissions · 4 cleared · Since 1992

Total

Cleared

Denied

Myriad Lase, Inc. has 4 FDA 510(k) cleared medical devices. Based in Forest Hill, US.

Historical record: 4 cleared submissions from 1992 to 1997. Primary specialty: General & Plastic Surgery.

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

Myriad Lase, 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 - Myriad Lase, Inc.

4 devices

1-4 of 4