Us Bionics, Inc. (Dba Suitx) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Us Bionics, Inc. (Dba Suitx) - FDA 510(k) Cleared Devices
Recent clearances: Phoenix
1
Total
1
Cleared
0
Denied
Us Bionics, Inc. (Dba Suitx) has 1 FDA 510(k) cleared medical devices. Based in Emeryville, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Us Bionics, Inc. (Dba Suitx) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Us Bionics, Inc. (Dba Suitx)
1 devices