Modus IR
Modus IR is a fluorescence imaging accessory used with the Synaptive Surgical Exoscope. With indocyanine green, it helps visualize vessels and blood flow in the cerebrovasculature before,…
Modus IR is a fluorescence imaging accessory used with the Synaptive Surgical Exoscope. With indocyanine green, it helps visualize vessels and blood flow in the cerebrovasculature before, during and after neurosurgery, plastic surgery and reconstructive surgery.
Light at selected wavelengths excites the imaging agent, which emits fluorescence detected by the optical system. This distinguishes structures containing the agent from surrounding tissue. The exoscope’s camera feed displays the resulting live images on the surgeon’s primary monitor and, optionally, a second monitor.
Listed Item
Surgical Exoscope Fluorescence Filter
Accessory Configuration
Authorized personnel enable Modus IR through software configuration management. Once enabled, a user-interface button activates fluorescence visualization. Indocyanine green is supplied separately from the accessory.
Who Else Makes It
Concentrated in Shanghai (2), Beijing (2), Guangdong (2).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Arthrex (Shanghai) Co., Ltd. | Shanghai | Shanghai | Exporter | 38 |
| GE Hangwei Medical Systems Co., Ltd. | Beijing | Beijing | Specification developer | 22 |
| GE Healthcare (China) Co., Ltd. | Beijing | Beijing | Specification developer | 22 |
| Scivita Medical Technology Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 19 |
| Siemens Shanghai, Medical Equipment Ltd. | Shanghai | Shanghai | Contract manufacturer | 10 |
| Guangdong Optomedic Technologies, Inc. | Foshan | Guangdong | Manufacturer | 7 |
| Zhuhai Dipu Medical Technology Co., Ltd. | Zhuhai | Guangdong | Manufacturer | 3 |
Record
| Listed by | Synaptive Medical Inc, Canada |
|---|---|
| FDA product code | IZI |
| Device type | System, X-Ray, Angiographic |
| Device class | Class 2 |
| Regulation | 21 CFR 892.1600 |
| Establishment | Manufacturer, Exporter |
| 510(k) | K231986 |
| Record published | 2024-04-02 |
| Record revised | 2025-08-06 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| SYN-0990 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Sterimed | Sterimed, Inc. | 114 |
| Med-Syringe | Argon Medical Devices, Inc. | 16 |
| Control Syringe | Argon Medical Devices, Inc. | 14 |
| Novadaq and Pinpoint | Novadaq Technologies, Inc. | 12 |
| DeRoyal | Deroyal Industries, Inc. | 12 |
| Namic | Navilyst Medical, Inc. | 9 |
| Namic | Medline Industries, Inc. | 8 |
| iMRX System | Imris Imaging, Inc. | 6 |
| System, X-Ray, Angiographic | B. Braun Medical Inc. | 4 |
| System, X-Ray, Angiographic | Intuitive Surgical, Inc. | 3 |
| Leica FL800 | Leica Microsystems (Schweiz) AG | 3 |
| Infrared 800 with Flow® 800 Option | Carl Zeiss Meditec Inc | 2 |
Showing 12 of 51. All products under System, X-Ray, Angiographic
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K231986 | 2024-03-25 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.