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Sign in to claim this brandVasorum, Ltd.
US
Last updated May 23, 2026
What Vasorum, Ltd. makes
Vasorum, Ltd. manufactures implantable vascular closure clips, specifically the Celt ACD Vascular Closure Device and its variants, including the Celt ACD PLUS series. These devices are available in multiple sizes, such as 5F, 6F, and 7F, with some models featuring an ESP (enhanced sheath profile) designation.
The devices are classified as Class III medical devices and are listed in the FDA’s Premarket Approval (PMA) database and the FDA’s Unique Device Identification (UDI) system. The company 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 type of medical devices does Vasorum, Ltd. manufacture?
Vasorum, Ltd. manufactures implantable vascular closure clips, specifically the Celt ACD Vascular Closure Device and its variants, including the Celt ACD PLUS series. These devices are designed for use in vascular procedures and are available in multiple sizes such as 5F, 6F, and 7F, with some models featuring an enhanced sheath profile (ESP) designation.
Where is Vasorum, Ltd. based?
Vasorum, Ltd. is based in the United States, as stated in the provided device data summary. The company’s location is explicitly noted in the SUMMARY section, which confirms its U.S. base without referencing any other geographic details.
In which regulatory registries are Vasorum, Ltd.'s devices listed?
Vasorum, Ltd.'s devices are listed in the FDA’s Premarket Approval (PMA) database and the FDA’s Unique Device Identification (UDI) system. This information is directly provided in the DEVICE DATA under the LISTED IN field, which specifies fda_pma and fda_udi as the registries where the devices appear.
How are Vasorum, Ltd.'s devices classified under regulatory frameworks?
Vasorum, Ltd.'s devices are classified as Class III medical devices. This classification is explicitly stated in the DEVICE CLASSES field of the provided data, indicating that these implantable vascular closure clips are subject to the highest level of regulatory control due to their potential risk and intended use.
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
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Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Celt ACD Vascular Closure Device 7F | KCLT-07 | FDA UDI | Class III | Active |
| Celt ACD Vascular Closure Device 6F_ESP | KCLT-06 | FDA UDI | Class III | Active |
| Celt ACD Vascular Closure Device 5F | KCLT-05 | FDA UDI | N/A | Active |
| Celt ACD PLUS Vascular Closure Device 5F | CLT-05 | FDA UDI | Class III | Active |
| Celt ACD PLUS Vascular Closure Device 6F | CLT-06 | FDA UDI | Class III | Active |
| Celt ACD PLUS Vascular Closure Device 7F | CLT-07 | FDA UDI | Class III | Active |
| Celt ACD Vascular Closure Device 5F_ESP | KCLT-05 | FDA UDI | Class III | Active |
| Celt ACD Vascular Closure Device 7F_ESP | KCLT-07 | FDA UDI | Class III | Active |
| Celt ACD Vascular Closure Device 6F | KCLT-06 | FDA UDI | Class III | Active |
| CELT ACD Vascular Closure Device | P150006 | FDA PMA | Class III | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Vasorum Dublin · IE FEI 3009984513