Data / Medical devices / Ireland / Vasorum
Vasorum: FDA-registered device maker in Dublin Dublin(County), Ireland, 1 PMA approval
Vasorum is registered with the FDA (registration 3009984513) in Dublin Dublin(County), Ireland. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated July 20, 2016. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009984513
- Address
- Trinitas House 2012, Orchard Avenue Citywest Business Campus, Dublin Dublin(County), Ireland, D24
- Owner or operator
- Vasorum Ltd (10052919)
- Roles
- Manufacturer, Specification developer
- First device listed
- October 18, 2016
- Registered through
- 2027
- Brand names listed
- Celt ACD PLUS Vascular Closure Device, Celt ACD Vascular Closure Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Hemostasis, Vascular | MGB | 3 | Manufacturer, Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| July 20, 2016 | P150006 | CELT ACD VASCULAR CLOSURE DEVICE | MGB | 4 | December 18, 2025 | accessdata.fda.gov |
Compare with other makers
Updated December 18, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.