Cogent - FDA 510(k) Cleared Devices

Cogent, is an Internet Service Provider operating one of the largest fiber-optic networks built for Internet traffic. The company maintains an FDA registered facility in Washington, DC, US.

Cogent's FDA 510(k) regulatory history reflects activity in General & Plastic Surgery devices. The company received 1 FDA 510(k) clearance from 1 total submission, with clearance granted in 1999. This represents a historical regulatory record, as the company has not received clearances in more than five years and is considered inactive in the medical device space.

The cleared device from this period was PARIETEX, a General & Plastic Surgery product. For detailed information on device names, product codes, and clearance dates, explore the full 510(k) database record.