A&D Company, Ltd. - FDA 510(k) Cleared Devices

A&D Company, Ltd. is a diversified manufacturer of precision measurement and medical devices with a manufacturing facility in San Jose, US. The company operates across test and measurement, weighing systems, inspection equipment, and medical device categories.

A&D Company has received 7 FDA 510(k) clearances from 7 total submissions, with all cleared devices in the Cardiovascular category. The company's regulatory activity spans from 2011 to 2022. This represents a historical record; no clearances have been submitted in recent years.

The company's Cardiovascular device portfolio focuses on digital blood pressure monitors for both professional and personal use. Notable cleared devices include the A&D Medical UM-212BLE, UB-1100BLE UltraConnect, and UA-1200BLE UltraConnect models, along with the TM-2657 family of digital blood pressure monitors.

Explore the complete regulatory history, device names, product codes, and clearance dates in the database records below.