C.R. Bard, Inc. (contract manufacturer, Queensbury, NY): 2 new FDA device listings, incl. introducer, catheter
C.R. Bard, Inc. (Queensbury, New York): 2 new FDA device listings, incl. introducer, catheter. Its amount of 2 is above the median of 1 (69th percentile). Dated 160 days ago, it serves as a historical benchmark. Score 65/100. 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: 55 related NY DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | C.R. Bard, Inc. |
| Owner / operator | C. R. Bard, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Queensbury, NY, US |
| New listings | 2 |
| Devices | Introducer, Catheter; Electrode, Pacemaker, Temporary |
| Product codes | DYB, LDF |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | GOETZ Temporary Pacing Electrode Catheter; Balloon Bipolar Temporary Pacing Electrode Catheter; Semi-Floating Temporary Pacing Electrode Catheter; NBIH Temporary Pacing Electrode Catheter; Balloon Bipolar Temporary Pacing Electrode Catheter, Right Heart Curve |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-05-28 |
| FDA registration number | 1313046 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (56 NY 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: 2026-05-28
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (NY first): Sterigenics U.S., LLC (contract sterilizer, Queensbury, NY) · Endure Industries, Inc. (specification developer, Homer, NY) · Premium Plus Dental Supplies Inc (other, Brooklyn, NY) · Siemens Healthcare Diagnostics Inc. (specification developer · Safetec Of America, Inc. (manufacturer, Buffalo, NY) · Browse all by state and category →
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: C.R. Bard, Inc. and 56 New York peers
- New York DeviceEstablishmentPulse records like this one: 56
- C.R. Bard, Inc.'s amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every New York peer: $11,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for C.R. Bard, Inc. in Queensbury, New York?
C.R. Bard, Inc. (Queensbury, NY), a contract manufacturer, added 2 FDA device listings on 2026-05-28.
How does C.R. Bard, Inc. compare to other New York DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 160 days old; check the official source for later updates before acting.
C.R. Bard, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| C.R. Bard, Inc. | Queensbury, NY | 2 | 69th | 2026-05-28 |
| 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 |
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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.