Valencia Technologies Corporation (manufacturer, Valencia, CA): 4 new FDA device listings, incl. stimulator, tibial, electrical, implantable, for urinary incontinence
Valencia Technologies Corporation (Valencia, California): 4 new FDA device listings, incl. stimulator, tibial, electrical, implantable, for urinary incontinence. Its amount of 4 is above the median of 1 (83rd percentile). Dated 188 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: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 283 related CA DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Valencia Technologies Corporation |
| Owner / operator | Boston Scientific Corporation |
| 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 | Valencia, CA, US |
| New listings | 4 |
| Devices | Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence; Instrument, Surgical, Non-Powered; General Surgery Tray; Dressing Change Tray |
| Product codes | QPT, HAO, LRO, OXQ |
| Device classes | Class I, Class II, Class III |
| Medical specialties | Neurology, General, Plastic Surgery, General Hospital |
| Brand names | eCoin Device Kit; eCoin Patient Kit; eCoin External Controller Kit |
| First new listing | 2026-05-01 |
| Latest new listing | 2026-05-01 |
| FDA registration number | 3010878085 |
| Registration expires | 2026-12-31 |
| amount percentile | 83th of 2,570 (median 1, 4.0x median) |
| Peer records CSV (284 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: 2026-05-01
- 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: Valencia Technologies Corporation and 284 California peers
- California DeviceEstablishmentPulse records like this one: 284
- Valencia Technologies Corporation's amount: 83rd percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every California peer: $56,800 (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 Valencia Technologies Corporation in Valencia, California?
Valencia Technologies Corporation (Valencia, CA), a manufacturer, added 4 FDA device listings on 2026-05-01.
How does Valencia Technologies Corporation compare to other California DeviceEstablishmentPulse records?
Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 188 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.
Valencia Technologies Corporation vs. top 2 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Valencia Technologies Corporation | Valencia, CA | 4 | 83rd | 2026-05-01 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
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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.