Oculus Optikgeraete GMBH
3 FDA 510(k) clearances · Recalling firm
◉ Watch Oculus Optikgeraete GMBH
| Record | Firm | Date |
|---|---|---|
| Oculus Pentacam AXL Wave, Ref 70020, CE 0123 recall (Z-2482-2023) | Oculus Optikgeraete GMBH | 2023-08-30 |
| Oculus Pentacam AXL , Ref 70100, CE 0123 recall (Z-2483-2023) | Oculus Optikgeraete GMBH | 2023-08-30 |
| Oculus Myopia Master , Ref 68100, CE 0123 recall (Z-2484-2023) | Oculus Optikgeraete GMBH | 2023-08-30 |
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Every clearance here is in the API, with alerts when new ones post.