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 15, 2026, FDA's public records list Rebound Therapeutics with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 27, 2023: Aurora Surgiscope System.
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.
| Oct 27, 2023 | Aurora Surgiscope SystemK232618 · GWG | 510(k) clearances |
| Dec 2, 2021 | AURORA Evacuator +CoagK203745 · GEI | 510(k) clearances |
| Nov 4, 2020 | Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box)K201840 · GWG | 510(k) clearances |
| Aug 12, 2020 | Aurora Evacuator +CoagK201637 · GEI | 510(k) clearances |
| Dec 6, 2019 | Aurora Surgiscope SystemK191861 · GWG | 510(k) clearances |
| Feb 12, 2019 | Aurora EvacuatorK190075 · GEI | 510(k) clearances |
| Jan 18, 2019 | Aurora Surgiscope SystemK182211 · GWG | 510(k) clearances |
| Apr 9, 2018 | Aurora EvacuatorK180372 · GEI | 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
