Optech, Inc. is one of 9903 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POLYVUE 43 (OCUFILCON A) SPHERICAL, TORIC AND ASPHERICAL MULTIFOCAL HYDROPHILIC CONTACT LENSES FOR DAILY WEAR
2
Total
2
Cleared
0
Denied
Optech, Inc. is a historical medical device manufacturer specializing in ophthalmic devices. The company operated with a manufacturing facility in Grand Junction, Colorado. Optech developed soft contact lenses for daily wear, including multifocal and toric designs.
The company received 2 FDA 510(k) clearances from 2 total submissions between 1998 and 2001. Both submissions resulted in clearances, with all devices classified in the ophthalmic category. Optech is no longer active in FDA submissions and should be treated as a historical regulatory record.
Notable cleared products include soft contact lenses manufactured from polymacon and ocufilcon A materials. These lenses addressed both spherical and toric corrections for multifocal vision correction needs. Explore the complete device names, product codes, and clearance dates in the full regulatory database.
FDA 510(k) Regulatory Record - Optech, Inc.
2 devices