Menicon Co., Ltd., R&D Center (specification developer, Kasugai Aichi, JP): 2 new FDA device listings, incl. lenses, soft contact, daily wear
Menicon Co., Ltd., R&D Center (Kasugai Aichi): 2 new FDA device listings, incl. lenses, soft contact, daily wear. Its amount of 2 is above the median of 2 (69th percentile). Dated 43 days ago, it serves as a historical benchmark. Score 70/100. 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: 2 · 69th percentile of 2,709 DeviceEstablishmentPulse records · 1.0x 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 | Menicon Co., Ltd., R&D Center |
| Owner / operator | Menicon Co. Ltd. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Kasugai Aichi, JP |
| New listings | 2 |
| Devices | Lenses, Soft Contact, Daily Wear; Lens, Contact, (Disposable) |
| Product codes | LPL, MVN |
| Device classes | Class II |
| Medical specialties | Ophthalmic |
| Brand names | Miru 1day UpSide (1 Day SiHy) |
| First new listing | 2026-09-23 |
| Latest new listing | 2026-09-23 |
| FDA registration number | 3003062331 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,709 (median 2, 1.0x 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: 2026-09-23
- 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: Menicon Co., Ltd., R&D Center and 61 JP peers
- JP DeviceEstablishmentPulse records like this one: 61
- Menicon Co., Ltd., R&D Center's amount: 69th 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)
70 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Menicon Co., Ltd., R&D Center in Kasugai Aichi?
Menicon Co., Ltd., R&D Center (Kasugai Aichi, JP), a specification developer (outsources manufacturing), added 2 FDA device listings on 2026-09-23.
How does Menicon Co., Ltd., R&D Center compare to other DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,709 records; the median is 2. It is 43 days old, still within a typical 45-day follow-up window. Its Score of 70/100 puts it among the stronger signals in this feed.
Menicon Co., Ltd., R&D Center vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Menicon Co., Ltd., R&D Center | Kasugai Aichi, JP | 2 | 69th | 2026-09-23 |
| Centinel Spine, LLC | West Chester, PA | 3 | 77th | 2026-10-22 |
| TORNIER Inc. | Columbia City, IN | 3 | 77th | 2026-10-21 |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI | 3 | 77th | 2026-10-14 |
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.