Eureka on the web
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The agent works the prompt against patents and technical literature, citing every source.
Run your analysis now →This landscape tracks patents at the intersection of shape-memory alloy materials — nitinol chiefly — and the safety and compliance claims built around them: biocompatibility, corrosion resistance, and medical device regulatory fit. The dataset is small and tightly focused, with all 18 published families sitting under surgical device classification rather than spread across a broad materials-science base.
Filing activity clusters around braided occluder frame design, with corrosion-safety and sterilisation language folded into those same device claims rather than filed independently. The result is a field where the dominant claim shape is well established, but the compliance layer underneath it is comparatively under-claimed.
Pick a task. Every answer cites the patents behind it.
Eighteen published families anchor this dataset, filed between 2015 and the 2026 cut-off, concentrated almost entirely in surgical device claims.
Filings rose from zero in 2017 to a peak of 6 in 2020, then dropped to zero at the 2022 midpoint before a partial uptick toward 2026. Because publication lags filing by roughly 18 months, the most recent years understate real activity — the apparent gap after 2020 should be checked against fresh priority-date data rather than read as a slowdown.
A61B (diagnosis and surgery) covers all 18 records, while A61L (sterilising and disinfecting) appears in only 3. Compliance and biocompatibility language is overwhelmingly filed as dependent claims inside device patents rather than as standalone process filings.
Shares are the percentage of the 18 records in scope. A patent can carry several IPC classes, so the shares add up to more than 100%.
This page is one run against one query. Ask Eureka your own question about shape-memory alloy safety and compliance and every answer comes back with the patent numbers behind it.
Try EurekaBraided occluding devices having an access passage and methods including the same are described herein. The occluding device includes a braided frame with an annular distal disc portion, a waist member, and an annular proximal disc portion defining a passageway through the braided frame, formed with a closed-end braid.Filed by St. Jude Medical, Cardiology Division, published 2024-02-29 as a continuation of the assignee's earlier occluder frame family.


| # | Publication no. | Patent title | Citations |
|---|---|---|---|
| 1 | US20210236138A1 | Frame and patch design for occluder with access passage | 18 |
| 2 | WO2021158559A1 | Frame and patch design for occluder with access passage | 14 |
| 3 | US20210059684A1 | Erosion mitigating occluder | 12 |
| 4 | US20210236102A1 | Occluder locking mechanisms | 8 |
| 5 | US20210059651A1 | Occluder including external skirt | 7 |
| 6 | EP3834738A2 | Erosion mitigating occluder | 1 |
Ranked by citation count within the searched corpus; older records accumulate citations by tenure, so treat this as a signal of influence rather than current importance.
Publication numbers are shown where the record carries one (6 of 6 rows); clicking a row searches Eureka by that number.
When you want the answer in the next five minutes.
The agent works the prompt against patents and technical literature, citing every source.
Run your analysis now →When it has to run inside your own pipeline.
Patent search, landscape analysis and assignee resolution as MCP tools. Drop them into any agent framework, or call REST directly.
Browse MCP servers →Three findings stand out once the filing trend, classification split and citation pattern are read together.
Filings moved from zero in 2017 to a peak of 6 in 2020, then fell to zero at the 2022 midpoint. That pattern reads more like a single wave of device development than sustained year-on-year investment, though the most recent years are understated by publication lag.
All 18 records sit under A61B surgical devices; only 3 also touch A61L sterilising and disinfecting. Corrosion-safety and biocompatibility claims are written as dependent limitations on device patents rather than pursued as independent compliance filings.
Thirteen of the recorded filings went through the United States, with a smaller EPO presence and a single PCT filing. That concentration suggests the regulatory and commercial priority for this claim set has been the US medical device market first.
Eureka can read the same corpus for gaps instead of for coverage: under-claimed branches adjacent to shape-memory alloy safety and compliance, with the prior art for and against each one.
The assignee picture in this dataset is narrow enough that a single family lineage accounts for the most-cited records; the interesting signal is less about a competitive field and more about where nobody has filed yet.
Holds the most-cited records in the set, including the occluder frame family and its 2024 continuation, US20240065700A1. Latest-year filing volume is down 50% year-on-year, though this is one data point and should be checked against newer priority dates.
The bulk of records were filed through the United States Patent and Trademark Office, with a smaller EPO cohort and a single PCT filing, consistent with a US-market-first commercialisation approach for occluder devices.
Every record in the dataset falls under A61B, meaning there is no rival technology cluster (such as a standalone materials-science or coatings classification) competing for claim space here — the entire field is framed as surgical device engineering.
| Assignee | Recent year | YoY |
|---|---|---|
| St. Jude Medical, Cardiology Division, Inc. | 1 | -50% |
The filing pattern here raises specific follow-up questions rather than closing the topic off.
The drop to zero filings at the 2022 midpoint is very likely a publication-lag artefact rather than a real slowdown. Pulling priority-date records rather than publication-date records would clarify whether activity actually continued.
Run a priority-date search in EurekaThe dominant claim family turns on a specific combination of disc geometry, waist member and closed-end braid termination. A full claim chart against that boundary would show exactly how much design-around room exists in open-end or welded alternatives.
Build a claim chart in EurekaWith only 3 of 18 records touching A61L, a targeted prior-art search focused purely on corrosion-safety or biocompatibility methods, independent of any specific device, would confirm whether the white space read here holds up.
Search white space in EurekaIn this dataset, biocompatibility and corrosion-safety language is almost never filed as a standalone patent; only 3 of 18 records fall under A61L (sterilising and disinfecting), and those are typically dependent claims attached to a surgical device family under A61B. If you are searching for a freestanding biocompatibility-testing patent, expect to find it bundled inside occluder or implant device filings rather than as its own claim set. A targeted search should pull the full device family and read the dependent claims, not just the title.
The most-cited records in this set, including US20210236138A1 and its PCT counterpart WO2021158559A1, along with the more recent US20240065700A1, trace to St. Jude Medical, Cardiology Division. These cover braided frame geometry with distal and proximal disc portions, a waist member, and a closed-end braid termination. Competing or alternative designs in the same set use open-end braids, external skirts, or different locking mechanisms, which points to where design-around options currently sit.
The trend shows a peak of 6 filings in 2020 followed by a drop to zero at the 2022 midpoint, but this should not be read at face value. Publication typically lags actual filing by around 18 months, so filings made in 2024 and 2025 may not yet be visible in the public record. A genuine slowdown is possible, but the safer interpretation is that the post-2020 years are simply undercounted until more publications clear the pipeline.
A61B covers diagnostic and surgical instruments and devices, which is where all 18 records in this dataset sit, including occluder frames, locking mechanisms, and access-passage designs. A61L covers sterilising, disinfecting and biocompatibility-related subject matter, and only 3 of the 18 records touch it. Practically, this means the corrosion-safety and sterilisation methods relevant to shape-memory alloy devices are described as features of a specific device rather than filed as independent compliance processes.
Yes — the thin A61L coverage (3 of 18 records) against near-total A61B saturation suggests standalone corrosion-safety or sterilisation-method claims, decoupled from a specific device geometry, remain under-filed. The near-zero 2022 midpoint alongside a 2020 peak also warrants checking whether newer priority filings have quietly re-entered this space. Anyone filing a first claim there should tie it to a measurable corrosion-resistance or biocompatibility threshold rather than a specific frame design, to avoid overlapping the dominant occluder-frame claims already in force.
Go past this page: query the whole shape-memory alloy safety and compliance corpus yourself, in your own scope.
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Disclaimer. This page is generated from Patsnap Eureka data drawn from a limited snapshot of global patent and scientific-literature records, and is provided for general information and reference only.
Patent data carries inherent limitations: recent filings (typically the most recent 18–24 months) are under-counted due to standard publication lag; counts may be reported at either a patent-family or a patent-record basis and are not always directly comparable; classification, applicant-name, and citation data may contain errors, duplicates, or omissions; and the underlying search query defines and constrains the scope shown. As a result, the analysis may be incomplete or inaccurate and may not reflect the full technology landscape.
Nothing on this page constitutes an exhaustive prior-art, novelty, freedom-to-operate, or validity search, nor does it constitute legal, financial, investment, or professional advice, and it should not be relied upon as such. Any patent, commercial, or strategic decision should be verified independently and reviewed with qualified patent, legal, and domain professionals. Patsnap makes no warranties, express or implied, as to the accuracy, completeness, or fitness for any particular purpose of the information presented.
Machine translation. Assignee and organisation names originally recorded in Chinese, Japanese or Korean have been rendered into English by an AI translation step so that the tables stay readable. These renderings are best-effort and may not match a company's registered English name; the original name is what the underlying patent record carries, and it is what any Eureka query launched from this page uses.