Mim Software, Inc.
Mim Software, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 1 FDA device recall on record.
Top product codes for Mim Software, Inc.
FDA recalls by Mim Software, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Mim Software, Inc.
- K253270 — Contour ProtégéAI+
- K251883 — MIM LesionID Pro
- K250035 — Contour ProtégéAI+
- K243012 — MIM Symphony HDR Fusion
- K233620 — MIM - Centiloid Scaling
- K232862 — MIM Monte Carlo Dosimetry
- K232514 — MIM Dose Analysis
- K231765 — Contour ProtégéAI
- K223774 — Contour ProtégéAI
- K223800 — MIM Additional Tracers
- K220256 — MIM-Ablation
- K213976 — Contour ProtégéAI
- K210632 — Contour ProtegeAI
- K193252 — Contour ProtegeAI
- K190379 — MIM on Linux
- K182624 — MIM - MRT Dosimetry
- K180815 — MIM - SPECTRA Quant
- K172218 — MIM Y90 Dosimetry
- K151913 — MIM-Thin Client (mobile)
- K112930 — MOBILE MIM
- K103576 — MIM 5.2 (BRACHY)
- K103785 — MOBILE MIM
Data sourced from openFDA. This site is unofficial and independent of the FDA.