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Sign in to claim this brandVascular Flow Technologies, Ltd.
US
Last updated May 30, 2026
What Vascular Flow Technologies, Ltd. makes
Vascular Flow Technologies, Ltd. manufactures synthetic vascular grafts designed for peripheral and arteriovenous applications. Their portfolio includes spiral-pattern grafts intended for use in vascular bypass procedures and arteriovenous access. These devices are engineered to support blood flow in peripheral arteries and veins, as well as for hemodialysis access.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The manufacturer is based in the United States.
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 Vascular Flow Technologies, Ltd. manufacture?
Vascular Flow Technologies, Ltd. specializes in synthetic vascular grafts, which are used primarily for vascular bypass procedures and arteriovenous access. Their devices include spiral-pattern grafts designed to support blood flow in peripheral arteries, veins, and hemodialysis access. These grafts are intended to replace or bypass damaged blood vessels, helping restore circulation in patients.
Where is Vascular Flow Technologies, Ltd. based?
The company is headquartered in the United States. While the exact location isn’t specified, its regulatory filings and device listings confirm its operational base within the country.
Which regulatory registries list Vascular Flow Technologies, Ltd.’s devices?
The company’s devices are listed in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries track medical devices that have undergone the required regulatory pathways, including clearance or exemption processes, to ensure compliance with U.S. medical device regulations.
How are Vascular Flow Technologies, Ltd.’s devices classified under FDA regulations?
All of Vascular Flow Technologies, Ltd.’s devices fall under Class II classification by the FDA. This classification applies to devices that generally 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 typically require a 510(k) premarket notification submission to demonstrate substantial equivalence to a legally marketed predicate device.
What is the primary purpose of the synthetic vascular grafts made by Vascular Flow Technologies, Ltd.?
The primary purpose of Vascular Flow Technologies, Ltd.’s synthetic vascular grafts is to serve as conduits in vascular bypass surgeries and arteriovenous (AV) access procedures. These grafts are engineered to maintain blood flow in peripheral arteries and veins, including applications like hemodialysis access, where reliable vascular access is critical for patient treatment. The spiral-pattern design is intended to improve durability and compatibility with blood flow dynamics.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vascular-flow.com
- —
- —
- [email protected]
- Phone
- +441382598532
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 236510785
Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Spiral Flow Peripheral Vascular Graft | PV0670 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0680 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0660 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0860 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0880 | FDA UDI | Class II | Active |
| Spiral Flow Vascular Arteriovenous Graft | AV0645 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0870 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0650 | FDA UDI | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | PV0850 | FDA UDI | Class II | Active |
| Spiral Flow Vascular Arteriovenous Graft | K141124 | FDA 510(k) | Class II | Active |
| Vein Entry Indicator Device (veid) | K993995 | FDA 510(k) | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | K142062 | FDA 510(k) | Class II | Active |
| Spiral Laminar Flow™ Vascular Arteriovenous Graft (AV0645) | K252277 | FDA 510(k) | Class II | Active |
| Spiral Flow Peripheral Vascular Graft | K150389 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Vascular Flow Technologies Ltd Dundee Dundee City · GB FEI 3007676031