Becton, Dickinson & Co. (manufacturer, Sparks, MD): 2 new FDA device listings, incl. device for home collection and transport of vaginal specimens by lay u
Becton, Dickinson & Co. (Sparks, Maryland): 2 new FDA device listings, incl. device for home collection and transport of vaginal specimens by lay u. Its amount of 2 is above the median of 1 (69th percentile). Dated 146 days ago, it serves as a historical benchmark. Score 70/100. 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: 13 related MD DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Becton, Dickinson & Co. |
| Owner / operator | Becton Dickinson and Company |
| Role | Manufacturer |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | Sparks, MD, US |
| New listings | 2 |
| Devices | Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay; System, Blood Culturing |
| Product codes | SEP, MDB |
| Device classes | Class I, Class II |
| Medical specialties | Microbiology |
| Brand names | Onclarity Self-Collection Kit-Viper LT; Onclarity Self-Collection Kit-COR; BD BACTEC FXI Culture System Workflow Module; BD BACTEC FXI Culture System Analyzer Module; BD BACTEC FXI 480/960 Culture System Software |
| First new listing | 2026-05-29 |
| Latest new listing | 2026-06-11 |
| FDA registration number | 1119779 |
| Registration expires | 2027-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (14 MD 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: 2026-06-11
- 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: Becton, Dickinson & Co. and 14 Maryland peers
- Maryland DeviceEstablishmentPulse records like this one: 14
- Becton, Dickinson & Co.'s amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Maryland peer: $2,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Becton, Dickinson & Co. in Sparks, Maryland?
Becton, Dickinson & Co. (Sparks, MD), a manufacturer, added 2 FDA device listings between 2026-05-29 and 2026-06-11.
How does Becton, Dickinson & Co. compare to other Maryland DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 146 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Becton, Dickinson & Co. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Becton, Dickinson & Co. | Sparks, MD | 2 | 69th | 2026-06-11 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
| INNO Holdings Inc. | Millcreek, UT | 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.