Signature Orthopaedics Europe Ltd (manufacturer, Athlone Westmeath, IE): 4 new FDA device listings, incl. prosthesis, hip, constrained, cemented or uncemented, metal/polymer
Signature Orthopaedics Europe Ltd (Athlone Westmeath): 4 new FDA device listings, incl. prosthesis, hip, constrained, cemented or uncemented, metal/polymer. Its amount of 4 is above the median of 1 (83rd percentile). Dated 156 days ago, it serves as a historical benchmark. Score 75/100. 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: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x 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 | Signature Orthopaedics Europe Ltd |
| Owner / operator | Signature Orthopaedics Pty Limited |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Athlone Westmeath, IE |
| New listings | 4 |
| Devices | Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Product codes | KWZ, JDI, MEH, LPH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Evolve AP Cup |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-06-01 |
| FDA registration number | 3014763043 |
| Registration expires | 2026-12-31 |
| amount percentile | 83th of 2,570 (median 1, 4.0x 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: 2026-06-01
- 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: Signature Orthopaedics Europe Ltd and 20 IE peers
- IE DeviceEstablishmentPulse records like this one: 20
- Signature Orthopaedics Europe Ltd's amount: 83rd 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)
75 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Signature Orthopaedics Europe Ltd in Athlone Westmeath?
Signature Orthopaedics Europe Ltd (Athlone Westmeath, IE), a manufacturer, added 4 FDA device listings on 2026-06-01.
How does Signature Orthopaedics Europe Ltd compare to other DeviceEstablishmentPulse records?
Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 156 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Signature Orthopaedics Europe Ltd vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Signature Orthopaedics Europe Ltd | Athlone Westmeath, IE | 4 | 83rd | 2026-06-01 |
| Piraeus Medical, Inc. | Maple Grove, MN | 4 | 83rd | 2026-10-12 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
Related records
DeviceEstablishmentPulse: 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.