Company ยท US
Exo, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 2025. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|
| QIH | Automated Radiological Image Processing Software | 3 |
| FIQ | Cannula, A-V Shunt | 1 |
| MYN | Analyzer, Medical Image | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|
| Apr 24, 2025 | K243239 | Lung AI (LAI001) Exo, Inc. | MYN |
| Nov 20, 2024 | K242359 | Strain AI (SAI001) Exo, Inc. | QIH |
| Nov 17, 2023 | K232501 | AI Platform (AIP001) Exo, Inc. | QIH |
| Jun 22, 2023 | K230497 | Bladder AI (AIBV01) Exo, Inc. | QIH |
| Jul 7, 1983 | K831801 | HEMOCLAV VENOUS CATHETER Exo, Inc. | FIQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|
| No recalls in this window. |