Zeus Scientific LLC (manufacturer, Branchburg, NJ): 7 new FDA device listings, incl. extractable antinuclear antibody, antigen and control
Zeus Scientific LLC (Branchburg, New Jersey): 7 new FDA device listings, incl. extractable antinuclear antibody, antigen and control. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 64 days ago, it serves as a historical benchmark. Score 85/100. 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: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 48 related NJ DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Zeus Scientific LLC |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device |
| Location | Branchburg, NJ, US |
| New listings | 7 |
| Devices | Extractable Antinuclear Antibody, Antigen And Control; Anti-Ss-A Ro60 Autoantibodies; Anti-Ss-A 52 Autoantibodies; Devices, Measure, Antibodies To Glomerular Basement Membrane (Gbm); Test System, Antineutrophil Cytoplasmic Antibodies (Anca) |
| Product codes | LLL, PET, OBE, MVJ, MOB |
| Device classes | Class II |
| Medical specialties | Immunology |
| Brand names | Alegria Flash ENA Screen; Alegria Flash SSA-52; Alegria Flash SSA-60; Alegria FLash SSB; Alegria Flash MPO; Alegria Flash GBM; Alegria Flash PR3; Alegria Flash CTD Screen |
| First new listing | 2026-09-01 |
| Latest new listing | 2026-09-01 |
| FDA registration number | 2242436 |
| Registration expires | 2026-12-31 |
| amount percentile | 90th of 2,570 (median 1, 7.0x median) |
| Peer records CSV (49 NJ 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: 2026-09-01
- 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: Zeus Scientific LLC and 49 New Jersey peers
- New Jersey DeviceEstablishmentPulse records like this one: 49
- Zeus Scientific LLC's amount: 90th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every New Jersey peer: $9,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
85 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Zeus Scientific LLC in Branchburg, New Jersey?
Zeus Scientific LLC (Branchburg, NJ), a manufacturer, added 7 FDA device listings on 2026-09-01.
How does Zeus Scientific LLC compare to other New Jersey DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 64 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.
Zeus Scientific LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Zeus Scientific LLC | Branchburg, NJ | 7 | 90th | 2026-09-01 |
| Abyrx, Inc. | Stamford, CT | 7 | 90th | 2026-10-07 |
| Boston Scientific Corp., Marina Bay Cust. Fulfillment Center | Quincy, MA | 6 | 88th | 2026-10-16 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
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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.