Rodo Medical, Inc. is one of 12964 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rodo Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rodo Abutment System, Rodo Smilekey, RODO Abutment System
3
Total
3
Cleared
0
Denied
Rodo Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 3 cleared submissions from 2016 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Rodo Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and PaxMed International, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Rodo Medical, Inc.
3 devices