FDA applicant
Tva Medical, Inc.
FDA records 2 decisions for Tva Medical, Inc. (Austin, TX) from 2016 to 2018: 1 510(k) clearance and 1 De Novo grant. Most are in product codes PQK (Percutaneous Catheter For Creation Of An…) and GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Tva Medical, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2018
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2016.
Planning a device like Tva Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report