FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji (specification developer, KOKUBUNJI-SHI Tokyo, JP): 1 new FDA device listing, incl. transducer, ultrasonic, diagnostic

FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji (KOKUBUNJI-SHI Tokyo): 1 new FDA device listing, incl. transducer, ultrasonic, diagnostic. Its amount of 1 is above the median of 2 (50th percentile). Dated 84 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 15 published fields of this record are shown below. Locked: 60 related JP DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentFUJIFILM Corporation Medical Systems Research & Development Center Kokubunji
Owner / operatorFUJIFILM Corporation
RoleSpecification developer (outsources manufacturing)
Establishment typesDevelop Specifications But Do Not Manufacture At This Facility
LocationKOKUBUNJI-SHI Tokyo, JP
New listings1
DevicesTransducer, Ultrasonic, Diagnostic
Product codesITX
Device classesClass II
Medical specialtiesRadiology
Brand namesBA-004CC
First new listing2026-08-14
Latest new listing2026-08-14
FDA registration number3019784575
Registration expires2026-12-31
amount percentile50th of 2,709 (median 2, 0.5x median)
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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: 2026-08-14
  • 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: FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji and 61 JP peers

  • JP DeviceEstablishmentPulse records like this one: 61
  • FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji'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)

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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

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 FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji in KOKUBUNJI-SHI Tokyo?

FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji (KOKUBUNJI-SHI Tokyo, JP), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-08-14.

How does FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji 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 84 days old; check the official source for later updates before acting.

FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
FUJIFILM Corporation Medical Systems Research & Development Center KokubunjiKOKUBUNJI-SHI Tokyo, JP150th2026-08-14
Centinel Spine, LLCWest Chester, PA377th2026-10-22
TORNIER Inc.Columbia City, IN377th2026-10-21
Davol Inc., Sub. C.R. Bard, Inc.Warwick, RI377th2026-10-14

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.

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