Mizuho Corporation (foreign exporter, BUNKYO-KU Tokyo, JP): 1 new FDA device listing, incl. punch, surgical
Mizuho Corporation (BUNKYO-KU Tokyo): 1 new FDA device listing, incl. punch, surgical. Its amount of 1 is above the median of 2 (50th percentile). Dated 162 days ago, it serves as a historical benchmark. Score 25/100. 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.
| Field | Value |
|---|---|
| Establishment | Mizuho Corporation |
| Owner / operator | MIZUHO Corporation |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | BUNKYO-KU Tokyo, JP |
| New listings | 1 |
| Devices | Punch, Surgical |
| Product codes | LRY |
| Device classes | Class I |
| Medical specialties | General, Plastic Surgery |
| Brand names | 02-095-02 Kerrison Rongeur 150 x 3 mm, 35 deg, Upward; 02-095-08 Kerrison Rongeur 180 x 1 mm, 35 deg, Upward; 02-095-06 Kerrison Rongeur 180 x 4 mm, 35 deg, Upward; 02-095-04 Kerrison Rongeur 150 x 5 mm, 35 deg, Upward; 02-095-01 Kerrison Rongeur 150 x 2 mm, 35 deg, Upward; 02-095-05 Kerrison Rongeur 180 x 3 mm, 35 deg, Upward; 02-095-03 Kerrison Rongeur 150 x 4 mm, 35 deg, Upward; 02-095-07 Kerrison Rongeur 180 x 5 mm, 35 deg, Upward |
| First new listing | 2026-05-27 |
| Latest new listing | 2026-05-27 |
| FDA registration number | 3011547624 |
| Registration expires | 2027-12-31 |
| 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: 2026-05-27
- 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: Mizuho Corporation and 61 JP peers
- JP DeviceEstablishmentPulse records like this one: 61
- Mizuho 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)
25 / 100 Score
What is the DeviceEstablishmentPulse record for Mizuho Corporation in BUNKYO-KU Tokyo?
Mizuho Corporation (BUNKYO-KU Tokyo, JP), a foreign exporter, added 1 FDA device listing on 2026-05-27.
How does Mizuho 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 162 days old; check the official source for later updates before acting. Its Score of 25/100 is modest; treat it as background rather than a priority.
Mizuho Corporation vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Mizuho Corporation | BUNKYO-KU Tokyo, JP | 1 | 50th | 2026-05-27 |
| Imperial Optical, Inc | Town Of Mount Royal, Quebec, CA | 3 | 77th | 2026-10-22 |
| Kash Sales Inc. | Richmond Hill Ontario, CA | 8 | 90th | 2026-10-16 |
| Mka Medikal Ic Ve Dis Ticaret Sanayi Limited Sirketi | Cankaya Ankara, TR | 9 | 92nd | 2026-10-17 |
Related records
DeviceEstablishmentPulse: Foreign exporter 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.