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 14, 2026, FDA's public records list Phasor Health with 5 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Nov 21, 2025: LEGACY.
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.
| Nov 21, 2025 | LEGACYK252696 · HBG | 510(k) clearances |
| Nov 5, 2025 | EVAC-MRIK252514 · JXG | 510(k) clearances |
| Oct 31, 2025 | GREENK252060 · HBE | 510(k) clearances |
| Jul 9, 2025 | EZ-FIDUCIALSK250505 · HAW | 510(k) clearances |
| Jun 3, 2025 | EVACK243205 · JXG | 510(k) clearances |
| Mar 21, 2025 | Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35Class II · Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time. | Device recalls |
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
