Hill-Rom is one of 20709 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hill-Rom - FDA 510(k) Cleared Devices
Recent clearances: Hill-Rom Wireless Connectivity Module, TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2
2
Total
2
Cleared
0
Denied
Hill-Rom, is a healthcare company specializing in patient care solutions with a manufacturing facility in Batesville, Indiana. The company develops medical devices and equipment across multiple clinical care settings.
Hill-Rom has received 2 FDA 510(k) clearances from 2 total submissions. The company's regulatory focus centers on Physical Medicine devices, with clearances spanning 2013 to 2015. This represents a historical regulatory record; the company has not received clearances in more than five years.
Historical FDA 510(k) cleared devices include the Hill-Rom Wireless Connectivity Module and the TOTALCARE bed system line, which encompasses bariatric and specialized patient care platforms. These products reflect the company's emphasis on advanced bed systems and patient mobility solutions for clinical environments.
For detailed information on device names, product codes, and specific clearance dates, consult the FDA 510(k) database.
FDA 510(k) Regulatory Record - Hill-Rom
2 devices