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MIM SOFTWARE INC.

Last updated September 17, 2026

Information

Country: US
Address: 25800 Science Park Dr Ste 180, Cleveland, OH, 44122
Website: mimsoftware.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 216-455-0600
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3004363352
DUNS Number: 136977290

Catalogue (53)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
Mim	7.2	FDA UDI	Class II	Active
MIMcloud	2.13	FDA UDI	Class I	Active
Mim	7.4.70	FDA UDI	Class II	Active
Mobile MIM	4.1	FDA UDI	Class II	Unknown
Mim	7.4	FDA UDI	Class II	Active
ContourProtégéAI	1.3	FDA UDI	Class II	Active
MIMviewer	4.0	FDA UDI	Class II	Unknown
Mim	6.6	FDA UDI	Class II	Unknown
MIMviewer	3.6	FDA UDI	Class II	Unknown
Mim	7.3	FDA UDI	Class II	Active
Mim	6.5	FDA UDI	Class II	Unknown
Mobile MIM	4.2	FDA UDI	Class II	Active
MIMviewer	3.9	FDA UDI	Class II	Unknown
ContourProtégéAI - CT Liver	1.0	FDA UDI	Class II	Active
MIMviewer	3.7	FDA UDI	Class II	Unknown
Mim	7.0	FDA UDI	Class II	Unknown
Mobile MIM	4.0	FDA UDI	Class II	Unknown
ContourProtégéAI - CT Head and Neck	1.0	FDA UDI	Class II	Active
Mim	6.9	FDA UDI	Class II	Unknown
ContourProtégéAI - CT Abdomen	2.0	FDA UDI	Class II	Active
ContourProtégéAI - MR Prostate	1.0	FDA UDI	Class II	Active
ContourProtégéAI - CT Prostate	1.0	FDA UDI	Class II	Active
ContourProtégéAI - CT SurePlan MRT	1.0	FDA UDI	Class II	Active
ContourProtégéAI - CT Lung and Liver	2.0	FDA UDI	Class II	Active
Mim	6.7	FDA UDI	Class II	Unknown
Mim	7.1	FDA UDI	Class II	Unknown
ContourProtégéAI - CT Thorax	1.0	FDA UDI	Class II	Active
ContourProtégéAI	1.2	FDA UDI	Class II	Active
Mim	6.8	FDA UDI	Class II	Unknown
MIMcloud	2.12	FDA UDI	Class I	Unknown
MIMviewer	3.8	FDA UDI	Class II	Unknown
MIM - Centiloid Scaling	K233620	FDA 510(k)	Class II	Active
MIM on Linux	K190379	FDA 510(k)	Class II	Active
MIM – Y90 Dosimetry	K172218	FDA 510(k)	Class II	Active
MIM - SPECTRA Quant	K180815	FDA 510(k)	Class II	Active
MIM – Additional Tracers	K223800	FDA 510(k)	Class II	Active
Contour ProtégéAI+	K250035	FDA 510(k)	Class II	Active
MIM – Dose Analysis	K232514	FDA 510(k)	Class II	Active
Contour ProtégéAI	K213976	FDA 510(k)	Class II	Active
Contour ProtégéAI	K223774	FDA 510(k)	Class II	Active
Contour ProtegeAI	K210632	FDA 510(k)	Class II	Active
MIM-Thin Client (mobile)	K151913	FDA 510(k)	Class II	Active
Contour ProtégéAI+	K253270	FDA 510(k)	Class II	Active
MIM – LesionID Pro	K251883	FDA 510(k)	Class II	Active
MIM – Monte Carlo Dosimetry	K232862	FDA 510(k)	Class II	Active
Mobile Mim	K103785	FDA 510(k)	Class II	Active
Mobile Mim	K112930	FDA 510(k)	Class II	Active
Contour ProtégéAI	K231765	FDA 510(k)	Class II	Active
Mim 5.2 (brachy)	K103576	FDA 510(k)	Class II	Active
Contour ProtegeAI	K193252	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.