510(k) · Cleared
ClearedUltraclip II Wing and Ultraclip II Coil
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Inrad · NEU Marker, Radiographic, Implantable
Cleared on Jan 30, 2007 after a 96-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 4 later devices descend from it.
- Decided
- Jan 30, 2007
- Review
- 96 days
- Class
- Class II
- Product code
- NEU
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK063238 Ultraclip II Wing and Ultraclip II CoilInrad · 2007
- Descendant · cites it directly · 3 of its ownK090547 Ultraclip II US Wing and Coil, Models: 862017U, 864017UC.R. Bard, Inc. · 2009 · Recalled
- Descendant · 2 generations on · 2 of its ownK152510 UltraCor Twirl Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2016
- Descendant · 3 generations on · 1 of its ownK180061 UltraCor Twirl Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2018
- Descendant · 4 generations on · 0 of its ownK243642 UltraCor™ Twirl™ Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2025
Most influential descendants
Showing 4 of 4 · See all- K090547Ultraclip II US Wing and Coil, Models: 862017U, 864017UC.R. Bard, Inc. · 2009 · cites it directly3descendants
- K152510UltraCor Twirl Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2016 · 2 generations on2descendants
- K180061UltraCor Twirl Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2018 · 3 generations on1descendant
- K243642UltraCor™ Twirl™ Breast Tissue MarkerBard Peripheral Vascular, Inc. · 2025 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K063238 | Ultraclip II Wing and Ultraclip II Coil | Inrad | 2007 | — |
| +1 | K090547 | Ultraclip II US Wing and Coil, Models: 862017U, 864017U | C.R. Bard, Inc. | 2009 | 4 |
| +2 | K152510 | UltraCor Twirl Breast Tissue Marker | Bard Peripheral Vascular, Inc. | 2016 | — |
| +3 | K180061 | UltraCor Twirl Breast Tissue Marker | Bard Peripheral Vascular, Inc. | 2018 | — |
| +4 | K243642 | UltraCor™ Twirl™ Breast Tissue Marker | Bard Peripheral Vascular, Inc. | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2016 | 1 | 0 |
| 2018 | 1 | 0 |
| 2025 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NEU? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new NEU device
- #1 K240042 MOLLI 2 Systemscore 14.4 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K090547 | Ultraclip II US Wing and Coil, Models: 862017U, 864017U | 2009 | 3 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K090547 (C.R. Bard, Inc., 2009) has gone furthest, with 3 descendants of its own.
How does its category compare?
All NEU devicesNEU Marker, Radiographic, Implantable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · NEU
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NEU
99in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NEU
2in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · NEU
411in 2025
MAUDE reports naming product code NEU, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 4 | 94 | 0 | 5 |
| 2008 | 7 | 107 | 0 | 5 |
| 2009 | 4 | 70 | 0 | 30 |
| 2010 | 5 | 69 | 0 | 12 |
| 2011 | 3 | 145 | 1 | 18 |
| 2012 | 3 | 120 | 0 | 54 |
| 2013 | 7 | 49 | 0 | 60 |
| 2014 | 3 | 48 | 0 | 38 |
| 2015 | 7 | 111 | 0 | 120 |
| 2016 | 2 | — | 0 | 56 |
| 2017 | 4 | 115 | 1 | 69 |
| 2018 | 8 | 89 | 0 | 66 |
| 2019 | 5 | 149 | 0 | 58 |
| 2020 | 3 | 169 | 0 | 45 |
| 2021 | 3 | 46 | 0 | 82 |
| 2022 | 2 | — | 1 | 100 |
| 2023 | 4 | 136 | 0 | 142 |
| 2024 | 10 | 267 | 2 (1) | 247 |
| 2025 | 5 | 99 | 2 | 411 |
| 2026 | 1 | — | 2 | — |
What is it indicated for?
The intended use of the Ultraclip IIWING and Ultraclip IICOIL is to attach to soft breast tissue at the surgical site during an open surgical breast biopsy or a percutaneous breast biopsy to radiographically mark the location of the biopsy procedure.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K063238 · printed Nov 4, 2026
Cite this page
510(k) Report. “K063238: Ultraclip II Wing and Ultraclip II Coil.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K063238
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026