Tautona Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tautona Group - FDA 510(k) Cleared Devices
Recent clearances: TauTona Pneumoperitoneum Assist Device (TPAD)
1
Total
1
Cleared
0
Denied
Tautona Group has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Tautona Group Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Tautona Group
1 devices