Data / Medical devices / Ireland / Vantive Manufacturing Limited
Vantive Manufacturing Limited: FDA-registered device maker in SWINFORD Mayo, Ireland, 2 510(k) clearances
Vantive Manufacturing Limited is registered with the FDA (registration 9612168) in SWINFORD Mayo, Ireland. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 29, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9612168
- FEI number
- 3002806471
- Address
- Foxford Road, SWINFORD Mayo, Ireland, F12 YK73
- Owner or operator
- Vantive US Healthcare LLC (9038727)
- Roles
- Manufacturer
- First device listed
- September 27, 1983
- Registered through
- 2026
- Brand names listed
- Locking Titanium Adapter for Peritoneal Dialysis Catheter and Locking Cap for Peritoneal Dialysis Catheter Adapter, MiniCap with Povidone-Iodine Solution, Minicap Extended Life PD Transfer Sets, Short Nose Clamp for Outlet Port of Plastic Container, UltraClamp Tubing Clamp
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Clamp, Line | FKK | 1 | Manufacturer | accessdata.fda.gov |
| Set, Administration, For Peritoneal Dialysis, Disposable | KDJ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| October 29, 2015 | K152675 | EXTENDED LIFE CAPD TRANSFER SET, PERITONEAL DIALYSIS TITANIUM CATHETER ADAPTER AND LOCKING CAP FOR TITANIUM CATHETER ADAPTER | KDJ | Substantially Equivalent | Baxter Healthcare | accessdata.fda.gov |
| October 29, 2015 | K152129 | FlexiCap Disconnect Cap with Povidone-Iodine Solution, MiniCap with Povidone-Iodine Solution | KDJ | Substantially Equivalent | Baxter Healthcare Corporation | accessdata.fda.gov |
Compare with other makers
Updated October 29, 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.