Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Keya Medical Technology and its 1 subsidiaries with 2 510(k) clearances and 2 AI-enabled devices. The most recent is a 510(k) clearance dated Jun 4, 2026: DEEPVESSEL Plaque.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Keya Medical Technology and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 4, 2026 | DEEPVESSEL PlaqueK260497 · QIH | 510(k) clearances |
| Jun 4, 2026 | DEEPVESSEL PlaqueK260497 · Radiology | AI-enabled devices |
| Apr 1, 2022 | DEEPVESSEL FFRK213657 · PJA | 510(k) clearances |
| Apr 1, 2022 | DEEPVESSEL FFRK213657 · Cardiovascular | AI-enabled devices |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
