Honda Motor Company, Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Honda Motor Company, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Honda Walking Assist Device
1
Total
1
Cleared
0
Denied
Honda Motor Company, Ltd. is a global manufacturer with a manufacturing facility in Wako-Shi, Japan. The company is primarily known for automotive, motorcycle, and power equipment production.
Honda has received 1 FDA 510(k) clearance from 1 total submission. The company's FDA regulatory activity focused on Neurology devices, with clearance granted in 2018. This represents a historical regulatory record; Honda has not pursued additional FDA 510(k) submissions in recent years.
The cleared device was a walking assistance product designed to support mobility and neurological function. Explore the device name, product code, and clearance date in the full regulatory record.
510(k) submissions have been managed by American Honda Motor Company, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Honda Motor Company, Ltd.
1 devices