# Mizuho Corporation (foreign exporter, BUNKYO-KU Tokyo, JP): 1 new FDA device listing, incl. punch, surgical

**Score:** 25/100

| 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 |

## Why this score


Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
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.