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Sign in to claim this brandVeryan Medical, Ltd.
US
Last updated May 23, 2026
What Veryan Medical, Ltd. makes
Veryan Medical, Ltd. manufactures bare-metal peripheral artery stents designed for vascular interventions. The BioMimics 3D Vascular Stent System is intended to treat obstructions in peripheral arteries, improving blood flow in lower limb and other peripheral vascular conditions.
The company’s products fall under FDA Class III regulation, requiring Premarket Approval (PMA) or a Unique Device Identifier (UDI) listing. These devices are authorised 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 Veryan Medical, Ltd. manufacture?
Veryan Medical, Ltd. specializes in bare-metal peripheral artery stents. These devices are specifically designed for vascular interventions to treat obstructions in peripheral arteries, helping restore blood flow in conditions like peripheral arterial disease (PAD). The primary focus is on improving vascular health in lower limbs and other peripheral vascular areas.
Where is Veryan Medical, Ltd. based, and where are its devices authorised for use?
Veryan Medical, Ltd. is headquartered in the United States. Its devices are authorised for use in the U.S., where regulatory pathways like Premarket Approval (PMA) and Unique Device Identifier (UDI) listings apply. The company’s products are subject to FDA oversight due to their classification under Class III.
Which regulatory registries or databases list Veryan Medical, Ltd.’s devices?
Veryan Medical, Ltd.’s devices are listed in the FDA’s Premarket Approval (PMA) registry and the Unique Device Identifier (UDI) database. These registries ensure compliance with U.S. regulatory requirements for Class III devices, which include stents requiring rigorous pre-market authorisation before commercial distribution.
How are Veryan Medical, Ltd.’s devices classified under U.S. regulations?
Veryan Medical, Ltd.’s peripheral artery stents are classified as FDA Class III devices. This classification is due to their high-risk nature, as they are implanted within the body and directly support or sustain life, or are of substantial importance in preventing impairment of human health. Class III devices require stringent regulatory oversight, including Premarket Approval (PMA) or UDI listing, to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (33)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BioMimics 3D Vascular Stent System | 142122-11 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-06-150-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-07 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-05-100-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-07-080-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-05-125-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-06-060-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-05-080-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-06-080-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-05-060-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-03 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 144700-19 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-05 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-15 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-07-150-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-05-150-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-13 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-06 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-01 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-06-100-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 144700-05 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 144700-12 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-14 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-07-060-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-02 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-10 | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | 142122-09 | FDA UDI | Class III | Unknown |
| BioMimics 3D Vascular Stent System | BM3D-07-125-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-06-125-120-UN | FDA UDI | Class III | Active |
| BioMimics 3D Vascular Stent System | BM3D-07-100-120-UN | FDA UDI | Class III | Active |
| Swirlgraft Bypass And Vascular Access Grafts | K051312 | FDA 510(k) | Class II | Active |
| Swirlgraft Vascular Access Graft | K060741 | FDA 510(k) | Class II | Active |
| BioMimics 3D® Vascular Stent System | P180003 | FDA PMA | Class III | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Veryan Medical Limited Galway · IE FEI 3011632150