Medical Device Manufacturer · US , Cleveland , OH

Mim Software, Inc. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2011

Recent clearances: Contour ProtégéAI+, MIM – LesionID Pro, Contour ProtégéAI+

Total

Cleared

Denied

Mim Software, Inc. has 22 FDA 510(k) cleared radiology devices. Based in Cleveland, US.

Latest FDA clearance: Mar 2026. Active since 2011.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.

Mim Software, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mim Software, Inc.

22 devices

1-12 of 22

MIM – Symphony HDR Fusion

K243012 · LLZ

Radiology · 26d

Cleared May 20, 2024

MIM - Centiloid Scaling

K233620 · LLZ

Radiology · 189d

Cleared May 13, 2024

MIM – Monte Carlo Dosimetry

MIM – Additional Tracers

Mim Software, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mim Software, Inc.

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