Company ยท US
Corinth Medtech, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2023. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Feb 24, 2023 | K230205 | Veloxion System Corinth Medtech, Inc. | FJL |
| Jun 13, 2019 | K191341 | Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll S Corinth Medtech, Inc. | FJL |
| Jun 6, 2019 | K191335 | Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll S Corinth Medtech, Inc. | HIH |
| Apr 24, 2019 | K190113 | Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll S Corinth Medtech, Inc. | HIH |
| Mar 15, 2019 | K190099 | Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll S Corinth Medtech, Inc. | FJL |
| Jul 25, 2018 | K180752 | Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pol Corinth Medtech, Inc. | HIH |
| Mar 24, 2017 | K162979 | Veloxion System Corinth Medtech, Inc. | FJL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||