Lunit INSIGHT MMG (v1.1.10)
FDA 510(k) K260320 · Lunit, Inc.
Submission
- Device name
- Lunit INSIGHT MMG (v1.1.10)
- Applicant
- Lunit, Inc.
Seoul, KR - Received
- January 30, 2026
- Decision date
- April 23, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QDQ – Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.2090
- Specialty
- Radiology
A radiological computer assisted detection and diagnostic software for suspected lesions is an image processing device intended to aid in the detection, localization, and characterization of lesions suspicious for cancer on acquired medical images (e.g., mammography , MR, CT, ultrasound, radiography). The device detects, identifies and characterizes lesions suspicious for cancer based on…
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| K253796 | Lunit INSIGHT DBT (V1.2)QDQ · Traditional | Lunit, Inc. | 03/26/2026SE |
| K251474 | Median LCS (internal name) / eyonis LCS (trade name) (1.0)QDQ · Traditional | Median Technologies | 02/06/2026SE |
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| K243341 | Genius AI Detection 2.0QDQ · Traditional | Hologic, Inc. | 07/31/2025SE |
More from Hologic, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K253796 | Lunit INSIGHT DBT (V1.2)QDQ · Traditional | 03/26/2026SE |
| K242652 | Lunit INSIGHT DBT v1.1QDQ · Special | 10/04/2024SE |
| K231470 | Lunit INSIGHT DBTQDQ · Traditional | 11/06/2023SE |
| K211678 | Lunit INSIGHT MMGQDQ · Traditional | 11/17/2021SE |
| K211733 | Lunit INSIGHT CXR TriageQFM · Traditional | 11/10/2021SE |
Questions and answers
When was Lunit INSIGHT MMG (v1.1.10) cleared by the FDA?
Lunit INSIGHT MMG (v1.1.10) (K260320) received a 510(k) decision of Substantially Equivalent on April 23, 2026, 83 days after the submission was received.
What is the product code of K260320?
The FDA product code is QDQ – Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer, a Class II (moderate risk) device regulated under 21 CFR 892.2090.