Bard Peripheral Vascular, Inc. (contract manufacturer, Tempe, AZ): 2 new FDA device listings, incl. shunt, portosystemic, endoprosthesis
Bard Peripheral Vascular, Inc. (Tempe, Arizona): 2 new FDA device listings, incl. shunt, portosystemic, endoprosthesis. Its amount of 2 is above the median of 1 (69th percentile). Dated 37 days ago, it serves as a historical benchmark. Score 75/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 14 related AZ DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Bard Peripheral Vascular, Inc. |
| Owner / operator | C. R. Bard, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Develop Specifications But Do Not Manufacture At This Facility |
| Location | Tempe, AZ, US |
| New listings | 2 |
| Devices | Shunt, Portosystemic, Endoprosthesis; Instrument, Biopsy |
| Product codes | MIR, KNW |
| Device classes | Class II, Class III |
| Medical specialties | Gastroenterology, Urology |
| Brand names | Liverty TIPS Stent Graft; EnCor EnCompass Breast Biopsy and Tissue Removal System |
| First new listing | 2026-08-24 |
| Latest new listing | 2026-09-28 |
| FDA registration number | 2020394 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (15 AZ records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-09-28
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Bard Peripheral Vascular, Inc. and 15 Arizona peers
- Arizona DeviceEstablishmentPulse records like this one: 15
- Bard Peripheral Vascular, Inc.'s amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Arizona peer: $3,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
75 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Bard Peripheral Vascular, Inc. in Tempe, Arizona?
Bard Peripheral Vascular, Inc. (Tempe, AZ), a contract manufacturer, added 2 FDA device listings between 2026-08-24 and 2026-09-28.
How does Bard Peripheral Vascular, Inc. compare to other Arizona DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 37 days old, still within a typical 45-day follow-up window. Its Score of 75/100 puts it among the stronger signals in this feed.
Bard Peripheral Vascular, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Bard Peripheral Vascular, Inc. | Tempe, AZ | 2 | 69th | 2026-09-28 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Arizona
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.