Data / Medical devices / Ireland / Cosmo Technologies Ltd.
Cosmo Technologies Ltd.: FDA-registered device maker in Dublin 2 Dublin(County), Ireland, 1 510(k) clearance
Cosmo Technologies Ltd. is registered with the FDA (registration 3012099114) in Dublin 2 Dublin(County), Ireland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 3, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012099114
- Address
- Riverside II Sir John Rogersons Quay, Dublin 2 Dublin(County), Ireland, D02KV60
- Owner or operator
- Conventus Biomedical Solutions (10050218)
- Roles
- Specification developer
- First device listed
- October 21, 2015
- Registered through
- 2026
- Brand names listed
- Eleview, SIC 8000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Submucosal Injection Agent | PLL | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 3, 2015 | K150852 | SIC 8000 | PLL | Substantially Equivalent | Cosmo Technologies, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 3, 2015. 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.