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Sign in to claim this brandMIM SOFTWARE INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 25800 Science Park Dr Ste 180, Cleveland, OH, 44122
- Website
- mimsoftware.com
- —
- —
- [email protected]
- Phone
- 216-455-0600
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3004363352
- DUNS Number
- 136977290
Catalogue (53)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MIM-Ablation | K220256 | FDA 510(k) | Class II | Active |
| MIM - MRT Dosimetry | K182624 | FDA 510(k) | Class II | Active |
| MIM – Symphony HDR Fusion | K243012 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 19, 2025 | Z-1267-2025 | — | open, classified | In situations where two images with differing Fields of View (FOV) complete an image fusion, an incorrect, elevated Maximum Standardized Uptake Value (SUV) within MIM Software versions 7.2.0 through 7.2.6.could result. |