Medical Device Manufacturer · US , Batesville , TN

Hill-Rom, Inc. - FDA 510(k) Cleared Devices

33 submissions · 33 cleared · Since 1986

Total

Cleared

Denied

Hill-Rom, Inc. is a global medical device manufacturer specializing in hospital care equipment and patient handling solutions. The company operates with a manufacturing facility in Batesville, Indiana, and serves healthcare providers across multiple care settings including hospitals, surgical centers, and home healthcare environments.

Hill-Rom has received 33 FDA 510(k) clearances from 33 total submissions since its first clearance in 1986. The company's regulatory portfolio focuses on General Hospital devices, including patient beds, stretchers, warming systems, and fluid management equipment. The latest clearance on record dates to 2021, reflecting the company's historical involvement in acute care and procedural device development.

Recent FDA 510(k) cleared devices include infant warmers, hospital beds, procedural stretchers, patient handling equipment, and vacuum-powered suction systems. These products demonstrate Hill-Rom's core expertise in patient mobility, thermal management, and clinical support technologies for hospital environments.

Explore the complete regulatory record, including device names, product codes, and clearance dates, to review Hill-Rom's full FDA 510(k) submission history.

FDA 510(k) Regulatory Record - Hill-Rom, Inc.

33 devices

1-12 of 33