Company ยท US
Rebound Therapeutics
FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2023. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 27, 2023 | K232618 | Aurora Surgiscope System Rebound Therapeutics Corporation | GWG |
| Dec 2, 2021 | K203745 | AURORA Evacuator +Coag Rebound Therapeutics | GEI |
| Nov 4, 2020 | K201840 | Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) Rebound Therapeutics | GWG |
| Aug 12, 2020 | K201637 | Aurora Evacuator +Coag Rebound Therapeutics | GEI |
| Dec 6, 2019 | K191861 | Aurora Surgiscope System Rebound Therapeutics | GWG |
| Feb 12, 2019 | K190075 | Aurora Evacuator Rebound Therapeutics | GEI |
| Jan 18, 2019 | K182211 | Aurora Surgiscope System Rebound Therapeutics Corporation | GWG |
| Apr 9, 2018 | K180372 | Aurora Evacuator Rebound Therapeutics | GEI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||