Nihon Kohden Corp. (specification developer, SHINJUKU-KU Tokyo, JP): 5 new FDA device listings, incl. tape and bandage, adhesive
Nihon Kohden Corp. (SHINJUKU-KU Tokyo): 5 new FDA device listings, incl. tape and bandage, adhesive. Its amount of 5 is above the median of 2 (86th percentile). Dated 91 days ago, it serves as a historical benchmark. Score 75/100. 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: 5 · 86th percentile of 2,709 DeviceEstablishmentPulse records · 2.5x 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 | Nihon Kohden Corp. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | SHINJUKU-KU Tokyo, JP |
| New listings | 5 |
| Devices | Tape And Bandage, Adhesive; Standard Polysomnograph With Electroencephalograph; Stimulator, Photic, Evoked Response; Full-Montage Standard Electroencephalograph; Non-Normalizing Quantitative Electroencephalograph Software |
| Product codes | KGX, OLV, GWE, GWQ, OLT |
| Device classes | Class I, Class II |
| Medical specialties | General Hospital, Neurology |
| Brand names | BLUPRO Attachment Tape, YS-111P7; BLUPRO Attachment Tape; YS-111P7 (P263A); LS-940A-ARM; LS-940A; JE-940A, EEG Amplifier Unit; EEG-1260A Neurofax System; LS-940A-OLY |
| First new listing | 2026-06-05 |
| Latest new listing | 2026-08-06 |
| FDA registration number | 9611252 |
| Registration expires | 2026-12-31 |
| amount percentile | 86th of 2,709 (median 2, 2.5x 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: 2026-08-06
- Data refreshed: 2026-11-04
- 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, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Nihon Kohden Corp. and 61 JP peers
- JP DeviceEstablishmentPulse records like this one: 61
- Nihon Kohden Corp.'s amount: 86th 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)
75 / 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.
What is the DeviceEstablishmentPulse record for Nihon Kohden Corp. in SHINJUKU-KU Tokyo?
Nihon Kohden Corp. (SHINJUKU-KU Tokyo, JP), a specification developer (outsources manufacturing), added 5 FDA device listings between 2026-06-05 and 2026-08-06.
How does Nihon Kohden Corp. compare to other DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (86th percentile) of 2,709 records; the median is 2. It is 91 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Nihon Kohden Corp. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Nihon Kohden Corp. | SHINJUKU-KU Tokyo, JP | 5 | 86th | 2026-08-06 |
| Deka Research & Development Corp. | Manchester, NH | 5 | 86th | 2026-10-19 |
| Orthopediatrics, Corp | Warsaw, IN | 5 | 86th | 2026-09-28 |
| Alc Enterprises Inc | Brooklyn, NY | 4 | 83rd | 2026-10-18 |
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.