Data / Medical devices / Tricuspid Valve Repair Device, Percutaneously Delivered
Tricuspid Valve Repair Device, Percutaneously Delivered (NPS): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Tricuspid Valve Repair Device, Percutaneously Delivered (product code NPS, Class 3). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- NPS
- Device class
- 3
- Medical specialty
- Unknown
- Implant
- Yes
- Life sustaining or supporting
- Yes
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Singapore | 1 |
| Ireland | 1 |
Makers of Tricuspid Valve Repair Device, Percutaneously Delivered
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Abbott Medical | Saint Paul, MN, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Abbott Vascular | Menlo Park, CA, United States | Manufacturer, Manufacturer for export | 0 | 1 | 0 | 0 | api.fda.gov | |
| EDWARDS LIFESCIENCES (SINGAPORE) Pte Ltd | Changi South East, Singapore | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Edwards Lifesciences LLC | Irvine, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Edwards Lifesciences Ireland Limited | Limerick Munster, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Edwards Lifesciences LLC | Draper, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.