Thi Total Healthcare Innovation GmbH is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Thi Total Healthcare Innovation GmbH - FDA 510(k) Cleared Devices
Recent clearances: ViVi® Toga Premium, ViVi® Surgical Helmet System (ViVi® Helmet, ViVi® Helmet HPL, ViVi® Hood)
2
Total
2
Cleared
0
Denied
Thi Total Healthcare Innovation GmbH has 2 FDA 510(k) cleared medical devices. Based in Feistritz Im Rosental, AT.
Latest FDA clearance: May 2025. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Thi Total Healthcare Innovation GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Albert Rego, Ph.D. Consulting and Albert Rego PHD, Inc (D.B.A Rego Associates).
FDA 510(k) Regulatory Record - Thi Total Healthcare Innovation GmbH
2 devices