Sony Corporation (specification developer, Yokohama-shi Kanagawa, JP): 1 new FDA device listing, incl. laparoscope, general & plastic surgery
Sony Corporation (Yokohama-shi Kanagawa): 1 new FDA device listing, incl. laparoscope, general & plastic surgery. Its amount of 1 is above the median of 2 (50th percentile). Dated 71 days ago, it serves as a historical benchmark. Score 60/100. 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: 60 related JP DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Sony Corporation |
| 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 | Yokohama-shi Kanagawa, JP |
| New listings | 1 |
| Devices | Laparoscope, General & Plastic Surgery |
| Product codes | GCJ |
| Device classes | Class II |
| Medical specialties | Gastroenterology, Urology |
| Brand names | OEV-321MUH OLYMPUS LCD Monitor; OEV-271MUH OLYMPUS LCD Monitor; OEV-431MUH OLYMPUS LCD Monitor |
| First new listing | 2026-08-27 |
| Latest new listing | 2026-08-27 |
| FDA registration number | 3004091527 |
| Registration expires | 2026-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (61 JP 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: 2026-08-27
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (JP first): Olympus Medical Systems Corp. (specification developer, HACH · GE Healthcare Japan Corporation (manufacturer, HINO-SHI Toky · Fujifilm Corporation (manufacturer, ASHIGARAKAMI-GUN Kanagaw · FUJIFILM Healthcare Manufacturing Corporation Hanamaki Offic · FUJIFILM Healthcare Manufacturing Corporation Sano Office (m · 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: Sony Corporation and 61 JP peers
- JP DeviceEstablishmentPulse records like this one: 61
- Sony Corporation's amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every JP peer: $12,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
60 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Sony Corporation in Yokohama-shi Kanagawa?
Sony Corporation (Yokohama-shi Kanagawa, JP), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-08-27.
How does Sony Corporation compare to other DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 71 days old; check the official source for later updates before acting.
Sony Corporation vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Sony Corporation | Yokohama-shi Kanagawa, JP | 1 | 50th | 2026-08-27 |
| 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 |
Related records
DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: Foreign establishment
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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.