Medical device makerLabelled 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 13, 2026, FDA's public records list Innosys Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 14, 2024: INNOVERSE Navigation Instruments.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 14, 2024 | INNOVERSE Navigation InstrumentsK241082 · OLO | 510(k) clearances |
| Apr 19, 2024 | UniSpace® Stand-Alone C CageK234119 · OVE | 510(k) clearances |
| Feb 6, 2024 | INNOVERSE Spinal SystemK233960 · NKB | 510(k) clearances |
| Oct 26, 2023 | ANAX™ 5.5 Spinal SystemK231737 · NKB | 510(k) clearances |
| Mar 3, 2023 | Dyna Locking Trochanteric Nail™K221084 · HSB | 510(k) clearances |
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
