Apostle Inc. (specification developer, Pleasanton, CA): 1 new FDA device listing, incl. equipment, laboratory, general purpose, labeled or promoted for a spec
Apostle Inc. (Pleasanton, California): 1 new FDA device listing, incl. equipment, laboratory, general purpose, labeled or promoted for a spec. Its amount of 1 is above the median of 2 (50th percentile). Dated 45 days ago, it serves as a historical benchmark. Score 65/100. As of 2026-11-04, 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: 1 · 50th percentile of 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 309 related CA DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Apostle Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Pleasanton, CA, US |
| New listings | 1 |
| Devices | Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use |
| Product codes | LXG |
| Device classes | Class I |
| Medical specialties | Clinical Chemistry |
| Brand names | MagTouch 2000 Nucleic Acid Extraction Automation System (24-well); MagTouch 2000 Nucleic Acid Extraction Automation System (96-well) |
| First new listing | 2026-09-21 |
| Latest new listing | 2026-09-21 |
| FDA registration number | 3017583200 |
| Registration expires | 2026-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (310 CA 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: 2026-09-21
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (CA first): Icu Medical, Inc. (specification developer, San Clemente, CA · Innopex Limited (foreign exporter, Toronto Ontario, CA) · Innopex Limited (foreign exporter, Toronto Ontario, CA) · Citest Diagnostics Inc. (repackager or relabeler, VANCOUVER · Cgbio USA, Inc. (repackager or relabeler, Irvine, CA) · 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, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Apostle Inc. and 310 California peers
- California DeviceEstablishmentPulse records like this one: 310
- Apostle Inc.'s amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every California peer: $62,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Apostle Inc. in Pleasanton, California?
Apostle Inc. (Pleasanton, CA), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-09-21.
How does Apostle Inc. compare to other California DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 45 days old, still within a typical 45-day follow-up window.
Apostle Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Apostle Inc. | Pleasanton, CA | 1 | 50th | 2026-09-21 |
| Centinel Spine, LLC | West Chester, PA | 3 | 77th | 2026-10-22 |
| TORNIER Inc. | Columbia City, IN | 3 | 77th | 2026-10-21 |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI | 3 | 77th | 2026-10-14 |
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DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in California
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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.