Medimaging Integrated Solution, Inc (Miis)
Medimaging Integrated Solution, Inc (Miis) appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 23, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253217 | MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus | December 23, 2025 |
| K234113 | MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display S | May 1, 2024 |
| K223926 | VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box | October 6, 2023 |
| K214050 | ENT Nasopharyngoscope and Accessories | July 1, 2022 |
| K193188 | MiiS Horus Eye Anterior Camera | January 14, 2020 |
| K181260 | MiiS Horus Scope DPT 100 | June 21, 2019 |
| K170470 | Digital Eye Anterior Camera | October 6, 2017 |