Nipro Medical Industries Ltd. (contract manufacturer, TATEBAYASHI-SHI Gunma, JP): 2 new FDA device listings, incl. tubes, vials, systems, serum separators, blood collection
Nipro Medical Industries Ltd. (TATEBAYASHI-SHI Gunma): 2 new FDA device listings, incl. tubes, vials, systems, serum separators, blood collection. Its amount of 2 is above the median of 1 (69th percentile). Dated 147 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-10-28, 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: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x 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 | Nipro Medical Industries Ltd. |
| Owner / operator | Nipro Corporation |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | TATEBAYASHI-SHI Gunma, JP |
| New listings | 2 |
| Devices | Tubes, Vials, Systems, Serum Separators, Blood Collection; Set, Administration, Intravascular |
| Product codes | JKA, FPA |
| Device classes | Class II |
| Medical specialties | Clinical Chemistry, General Hospital |
| Brand names | BD Vacutainer® Safety-Lok Blood Collection Set; BD Vacutainer® Safety-Lok Blood Collection Set with Pre-Attached Hold |
| First new listing | 2026-06-11 |
| Latest new listing | 2026-06-11 |
| FDA registration number | 9611446 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x 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: 2026-06-11
- Data refreshed: 2026-10-28
- 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, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Nipro Medical Industries Ltd. and 61 JP peers
- JP DeviceEstablishmentPulse records like this one: 61
- Nipro Medical Industries Ltd.'s amount: 69th percentile of 2,570 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)
55 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Nipro Medical Industries Ltd. in TATEBAYASHI-SHI Gunma?
Nipro Medical Industries Ltd. (TATEBAYASHI-SHI Gunma, JP), a contract manufacturer, added 2 FDA device listings on 2026-06-11.
How does Nipro Medical Industries Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 147 days old; check the official source for later updates before acting.
Nipro Medical Industries Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Nipro Medical Industries Ltd. | TATEBAYASHI-SHI Gunma, JP | 2 | 69th | 2026-06-11 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
DeviceEstablishmentPulse: Contract manufacturer 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.