Bard Peripheral Vascular, Inc.: PMA approval for Liverty TIPS Stent Graft
Bard Peripheral Vascular, Inc. (Tempe, Arizona): PMA approval for Liverty TIPS Stent Graft. Dated 40 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 8 published fields of this record are shown below. Locked: 17 related AZ FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | Bard Peripheral Vascular, Inc. |
| Product | Liverty TIPS Stent Graft |
| Generic / ingredient | SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS |
| Approval | PMA original approval (new class III device) |
| Application | P250050 |
| Decided | 2026-09-25 |
| Panel / class | Cardiovascular |
| Sponsor location | Tempe, AZ |
| Peer records CSV (18 AZ records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-09-25
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT
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Peer benchmark and outreach value: Bard Peripheral Vascular, Inc. and 18 Arizona peers
- Arizona FdaApprovalPulse records like this one: 18
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Arizona peer: $3,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
55 / 100 Score
- A new product launch.
What is the FdaApprovalPulse record for Bard Peripheral Vascular, Inc. in Tempe, Arizona?
The FDA approved Liverty TIPS Stent Graft (P250050) for Bard Peripheral Vascular, Inc. on 2026-09-25: PMA original approval (new class iii device).
How does Bard Peripheral Vascular, Inc. compare to other Arizona FdaApprovalPulse records?
It is 40 days old, still within a typical 45-day follow-up window.
Bard Peripheral Vascular, Inc. vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Bard Peripheral Vascular, Inc. | Tempe, AZ | 2026-09-25 |
| Vivasure Medical , Ltd. | Galway | 2026-10-16 |
| Edwards Lifesciences, LLC | Irvine, CA | 2026-10-01 |
| Rejoni, Inc. | Bedford, MA | 2026-09-28 |
Related records
FdaApprovalPulse: PMA original approval (new class III device) FdaApprovalPulse: records in Arizona
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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.