Benq Corporation - FDA 510(k) Cleared Devices

Benq Corporation, is a Taiwan-based technology company with a manufacturing facility in Taipei. The company manufactures displays, projectors, and lighting solutions for professional and consumer markets.

Benq received 1 FDA 510(k) clearance from 1 total submission in the Radiology device category. The cleared device was an LCD monitor (MD310C, MD310G, MD210G) intended for radiology applications. The company's FDA regulatory activity occurred in 2017. Benq has not submitted additional 510(k) applications since that time and is considered inactive in the FDA medical device clearance process.

This profile represents a historical regulatory record. For current product information and FDA device status, consult the FDA's 510(k) database directly using the device model numbers and clearance dates provided.