Merit Medical Ireland, Ltd (contract manufacturer, Galway Galway(County), IE): 5 new FDA device listings, incl. wire, guide, catheter
Merit Medical Ireland, Ltd (Galway Galway(County)): 5 new FDA device listings, incl. wire, guide, catheter. Its amount of 5 is above the median of 1 (87th percentile). Dated 76 days ago, it serves as a historical benchmark. Score 70/100. 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 19 related IE DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Merit Medical Ireland, Ltd |
| Owner / operator | Merit Medical Systems, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Galway Galway(County), IE |
| New listings | 5 |
| Devices | Wire, Guide, Catheter; Catheter, Embolectomy; Dilator, Vessel, For Percutaneous Catheterization |
| Product codes | DQX, DXE, DRE |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | MAK Nitinol/Gold-Tungsten Guide Wire; Needle's Eye Snare Retrieval Set; Curved Inner Femoral Sheath and Curved Introducer Sheath Set - Femoral.; InQwire Amplatz (IQA) |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-08-20 |
| FDA registration number | 9616662 |
| Registration expires | 2026-12-31 |
| amount percentile | 87th of 2,570 (median 1, 5.0x median) |
| Peer records CSV (20 IE 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: 2026-08-20
- 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: Merit Medical Ireland, Ltd and 20 IE peers
- IE DeviceEstablishmentPulse records like this one: 20
- Merit Medical Ireland, Ltd's amount: 87th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every IE peer: $4,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Merit Medical Ireland, Ltd in Galway Galway(County)?
Merit Medical Ireland, Ltd (Galway Galway(County), IE), a contract manufacturer, added 5 FDA device listings between 2026-05-28 and 2026-08-20.
How does Merit Medical Ireland, Ltd compare to other DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 76 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Merit Medical Ireland, Ltd vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Merit Medical Ireland, Ltd | Galway Galway(County), IE | 5 | 87th | 2026-08-20 |
| NGInstruments, Inc dba Avalign Cutting Instruments | Warsaw, IN | 4 | 83rd | 2026-10-16 |
| Cook Medical LLC | Bloomington, IN | 4 | 83rd | 2026-10-13 |
| Swiss-American CDMO,LLC | Carrollton, TX | 4 | 83rd | 2026-10-12 |
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.