Cooper Lasersonics, Inc. - FDA 510(k) Cleared Devices

Cooper Lasersonics, Inc. is a medical device manufacturer based in Orangeburg, US, specializing in laser surgical systems.

The company has received 52 FDA 510(k) clearances from 54 total submissions since its first clearance in 1982. Cooper Lasersonics focused primarily on CO2 and Nd:YAG laser systems for surgical applications across multiple specialties, including general and plastic surgery, otolaryngology, gastroenterology, and neurosurgery. The company's regulatory activity concluded in 1988, making this a historical record of its contributions to surgical laser technology.

Cooper Lasersonics is no longer active in FDA submissions. This profile documents the company's historical regulatory clearances and device portfolio for reference purposes.

Explore the complete list of device names, product codes, and clearance dates in the full regulatory record.