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Sign in to claim this brandVERAN MEDICAL TECHNOLOGIES INC.
US
Last updated May 24, 2026
What VERAN MEDICAL TECHNOLOGIES INC. makes
Veran Medical Technologies Inc. manufactures endoscopic control and video-imaging systems, including video processors, navigation systems, and steerable catheters with real-time tip tracking. Their portfolio includes image-guided systems for bronchoscopy, such as the SPiN Vision Video Bronchoscope System and the IG4 Endobronchial Navigation System, along with accessories like navigation guidewires and aspiration needles. These devices are designed for precise procedural guidance in thoracic and endobronchial applications.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and UDI databases. These systems are intended for use in the United States, where the manufacturer is based.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Veran Medical Technologies Inc. primarily manufacture?
Veran Medical Technologies Inc. specializes in endoscopic control and video-imaging systems. Their portfolio includes video processors, navigation systems, and steerable catheters with real-time tip tracking. The most common category is endoscopic control/video-imaging systems, such as the SPiN Vision Video Bronchoscope System and the IG4 Image-Guided System, which are designed for precise procedural guidance in thoracic and endobronchial applications.
Where is Veran Medical Technologies Inc. based, and where are their devices intended for use?
Veran Medical Technologies Inc. is based in the United States. Their devices are developed and marketed with a focus on the U.S. market, where they are intended for clinical use.
Which regulatory registries list Veran Medical Technologies Inc.’s devices?
Veran Medical Technologies Inc.’s devices are listed in the FDA’s 510(k) and UDI (Unique Device Identification) databases. These registries track medical devices that have undergone the necessary regulatory pathways, such as the 510(k) premarket notification process, to demonstrate substantial equivalence to legally marketed devices.
How are Veran Medical Technologies Inc.’s devices classified under FDA regulations?
Veran Medical Technologies Inc.’s devices fall under Class II classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls—such as performance standards, post-market surveillance, or labeling requirements—to ensure their safety and effectiveness. Class II devices are subject to premarket notification (510(k)) submissions to demonstrate compliance with these controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 181714804
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