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Search APP name SmartUSG WirelessUSG WirelessUSG Flash BladderUSG in Google Play, Apple Store to find.
SmartUSG Android
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WirelessUSG Flash iOS
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WirelessUSG Windows
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SmartUSG Android Version
Search SmartUSG in Google Play to download
You also can download SMARTUSG flash by this link
SmartUSG — New SONOSTAR Ultrasound APP
SmartUSG Android Version is a professional mobile application developed by SonoStar, designed to seamlessly integrate with the company’s AI-integrated ultrasound devices, enabling intuitive remote control, real-time imaging display and intelligent data analysis. Compatible with Android 9.0 and above, the APP supports wireless connection (5G/WiFi/Bluetooth) with SonoStar’s portable ultrasound probes and systems, breaking the limitations of traditional wired operation and facilitating flexible on-site diagnostics in clinics, emergency scenarios and grassroots medical institutions. Its core functions include multi-mode imaging control (B-mode, M-mode, Doppler), parameter adjustment (frequency, gain, depth), one-click image capture and video recording, as well as AI-assisted lesion labeling and preliminary analysis—leveraging the same advanced algorithms as SonoStar’s flagship systems to automatically identify typical lesions and generate preliminary diagnostic suggestions, reducing operational complexity for clinicians.
The APP features a user-friendly interface with customizable operation layouts, adapting to the usage habits of different medical professionals. It supports secure data storage and cloud synchronization, enabling clinicians to upload images and reports to designated medical platforms for remote consultation and case sharing, while complying with international medical data privacy standards (HIPAA, GDPR). Additionally, it integrates offline working mode, ensuring stable operation even in network-constrained areas, and offers built-in clinical guidelines and operation tutorials to assist grassroots medical staff in standardizing ultrasound examinations. Lightweight (less than 100MB) and energy-efficient, the APP runs smoothly on mainstream Android smartphones and tablets, perfectly matching SonoStar’s portable ultrasound devices to deliver a mobile, efficient and precise ultrasound diagnostic experience, further advancing the accessibility of high-quality medical imaging services globally.
WirelessUSG Flash iOS Version
WirelessUSG Flash iOS Version is a professional, iOS-optimized APP exclusively developed by SonoStar for its wireless ultrasound probes, compatible with iOS 14.0+ (iPhone/iPad). Meticulously tailored to Apple’s ecosystem, it achieves seamless integration with iOS hardware and software, delivering ultra-smooth operation and stable performance. Supporting 5G/WiFi and Bluetooth dual wireless connections, it enables instant probe pairing in seconds, with a simple process of selecting the probe’s WiFi signal, entering the unique password, and confirming connection via the WiFi indicator.
Equipped with comprehensive clinical functions, it supports B-mode, M-mode, Color Doppler imaging, and adjustable parameters (gain, depth, focus) to optimize image quality. Advanced features include intelligent noise reduction, one-click freeze/capture, professional measurement tools, and AI-assisted lesion analysis powered by deep learning algorithms, enhancing diagnostic precision and efficiency. Prioritizing data security, it adopts Face ID login and complies with HIPAA/GDPR standards, supporting encrypted iCloud sync and DICOM transmission.
Lightweight (under 80MB) with an iOS-native interface, it adapts to various device sizes and suits clinic consultations, emergency on-site diagnostics, and grassroots services. Its offline working mode ensures stability in low-network environments, empowering clinicians with a portable, precise ultrasound solution tailored for Apple devices.
WirelessUSG Android/Windows
WirelessUSG Android/Windows Version is a versatile cross-platform application developed by SonoStar, seamlessly compatible with Android 9.0+ (smartphones/tablets) and Windows 10+ (laptops/desktops), designed to pair with the company’s wireless ultrasound probes. It supports dual wireless connection modes—5G/WiFi for high-speed, long-distance transmission and Bluetooth for instant pairing, enabling stable, lag-free real-time high-resolution imaging. The APP integrates comprehensive professional functions, including multi-mode imaging control (B-mode, M-mode, Color Doppler), adjustable parameters (gain, depth, focus), one-click image/video capture and playback, as well as AI-assisted lesion analysis and intelligent noise reduction, significantly simplifying operational workflows for clinicians.
Prioritizing data security and practicality, the APP complies with HIPAA and GDPR medical data privacy standards, supporting secure local storage, cloud synchronization and DICOM server transmission for convenient remote consultation and case sharing. Its user-friendly interface features customizable layouts, adapting to both mobile and desktop operation habits. Lightweight (under 100MB), it runs smoothly without occupying excessive device resources. Suitable for clinics, emergency on-site diagnostics, grassroots medical services and academic training, it delivers flexible, precise ultrasound solutions across dual systems, empowering healthcare professionals with efficient diagnostic tools and supporting the popularization of accessible medical imaging services.
The Software Development Kit (SDK) for SONOSTAR’s wirelessUSG APP is designed to enable developers to integrate the core functionalities of the wirelessUSG (Ultrasound) application into their own systems, facilitating customized development and seamless functional expansion. Below is the key information about the current SDK version:
Supported Operating Systems
- Android: Fully supported, compatible with mainstream Android versions, enabling integration with Android devices to access core capabilities.
- Windows: Available for download, supporting Windows 7 and above. Ideal for building PC-side interactive applications like ultrasound data analysis systems.
- iOS: Currently not open to the public. Updates will be announced via official channels once the launch plan is confirmed.
Download & Contact
To obtain the Windows version of the SDK or software, please contact us at contact@sonostargroup.com. For efficient support, specify your usage scenario (e.g., enterprise development, academic research) and technical requirements in your email.
Supplementary Notes
The SDK offers standardized APIs for stable, compatible integration. Technical documents (interface specifications, parameter descriptions) for Android and Windows versions are available upon request via the above email. We continuously optimize SDK functions and compatibility—follow SONOSTAR’s official announcements for updates, including potential iOS support.
SONOSTAR Certificates
SonoStar holds a suite of authoritative certifications, including ISO international quality system certifications and CE medical device certifications, fully complying with global regulatory standards for medical and industrial ultrasound equipment. Its products have passed FDA marketing clearance requirements, meeting strict acoustic output and safety standards. These certifications cover human, veterinary and industrial product lines, validating product quality, safety and reliability, and laying a solid foundation for its global market access and brand trust.
ISO 13485 Certificate
SonoStar has obtained the ISO 13485 Certificate, an authoritative international standard specifically for medical device quality management systems, issued by a certification body recognized by UKAS and IAF. This certification strictly covers the entire lifecycle of SonoStar’s ultrasound products, including R&D, design, production, quality control, and after-sales service, ensuring full compliance with global medical device regulatory requirements. By implementing the ISO 13485 system, SonoStar has established standardized quality control processes, realizing traceability of raw materials and production links, and effectively guaranteeing the consistency, safety, and reliability of its AI-integrated ultrasound probes and diagnostic systems.
As a “passport” to enter the global medical device market, this certification lays a solid foundation for SonoStar’s products to access European, American, Japanese and other international markets, accelerating its global market layout. Domestically, it also serves as a key plus for government procurement and hospital bidding, enhancing the brand’s credibility among customers and partners. The acquisition of the ISO 13485 Certificate fully reflects SonoStar’s adherence to quality-oriented development and its commitment to providing high-standard, reliable medical imaging solutions for global healthcare institutions.
FDA Approved Devices
SonoStar’s core human ultrasound devices have obtained FDA (U.S. Food and Drug Administration) approval, a rigorous certification overseen by the FDA’s Center for Devices and Radiological Health (CDRH) to ensure medical device safety and effectiveness. The approved product line includes AI-integrated portable ultrasound probes and diagnostic systems, covering clinical scenarios such as thyroid, cardiovascular, and obstetric imaging, all compliant with FDA’s premarket review and quality system regulation requirements.
To secure approval, these devices underwent stringent testing, including acoustic output safety, imaging accuracy verification, and long-term operational stability assessments, validating their non-invasiveness and diagnostic reliability. This certification grants SonoStar direct access to the U.S. medical market, a key milestone in its global expansion. It also enhances the brand’s credibility among international healthcare institutions, strengthening partnerships in North America and beyond. The FDA approval further underscores SonoStar’s commitment to meeting global regulatory standards and delivering high-quality medical imaging solutions to global patients.
MDR CE Certificate
SonoStar’s human ultrasound devices have obtained the MDR CE Certificate, complying with the EU Medical Device Regulation (MDR) 2017/745, the most rigorous medical device regulatory standard in Europe. Issued by a Notified Body designated by EU member states, this certification covers the full product lifecycle, from R&D and clinical evaluation to production and post-market surveillance, ensuring strict alignment with EU safety, performance and clinical benefit requirements.
The certification process involved rigorous scrutiny, including clinical file review by independent expert panels (per MDR Article 54) and comprehensive testing of device safety and performance. The CE mark is followed by the Notified Body’s unique identification number, affirming compliance. This certification serves as a mandatory “market access pass” for the EU and EEA regions, enabling SonoStar to legally market its AI-integrated ultrasound probes and systems across 30+ European countries. It further enhances the brand’s global credibility, reinforcing its position as a compliant and reliable partner for healthcare institutions worldwide
Please contact with contact@sonostargroup.com to get the latest certificates
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