Company ยท FI
Disior, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2021 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (1 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 26, 2026 | K253764 | ENOS Software Guided External Fixation System Disior, Ltd. | OSN |
| Sep 29, 2025 | K250023 | SMART PCFD Disior, Ltd., FI | QIH |
| Jul 2, 2024 | K240736 | SMART Bun-Yo-Matic X-Ray Disior, Ltd., FI | QIH |
| Jun 20, 2024 | K240642 | SMART Bun-Yo-Matic CT Disior, Ltd., FI | QIH |
| Dec 8, 2023 | K223757 | Bonelogic Disior, Ltd., FI | QIH |
| Feb 5, 2021 | K203290 | Bonelogic Disior, Ltd., FI | LLZ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||