510(k) · Cleared
ClearedItclamp 50
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Innovative Trauma Care, Inc. · DXC Clamp, Vascular
Cleared on Oct 28, 2013 as substantially equivalent to K012219 (Aesculap, Inc., 2001) after a 63-day review. Its family tree reaches back 2 generations to 1989. 2 later devices descend from it.
- Decided
- Oct 28, 2013
- Review
- 63 days
- Class
- Class II
- Product code
- DXC
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K890443 (1989). 4 ancestors in all. 2 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK890443 Caspar Scalp Clip, ApplierAesculap Instruments Corp. · 1989
- 1 generation backK012219 Scalpfix Clip SystemAesculap, Inc. · 2001
- This deviceK132651 Itclamp 50Innovative Trauma Care, Inc. · 2013
- Descendant · cites it directly · 1 of its ownK140805 Itclamp 50Innovative Trauma Care, Inc. · 2014
- Descendant · 2 generations on · 0 of its ownK150813 iTClamp50Innovative Trauma Care, Inc. · 2015
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K890443 | Caspar Scalp Clip, Applier | Aesculap Instruments Corp. | 1989 | — |
| −1 | K012219 | Scalpfix Clip System | Aesculap, Inc. | 2001 | — |
| 0 (this device) | K132651 | Itclamp 50 | Innovative Trauma Care, Inc. | 2013 | — |
| +1 | K140805 | Itclamp 50 | Innovative Trauma Care, Inc. | 2014 | — |
| +2 | K150813 | iTClamp50 | Innovative Trauma Care, Inc. | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 1 | 0 |
| 1994 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2015 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in DXC? 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 DXC device
- #1 K262086 PreludeSYNC™ Radial Compression Devicescore 13.5 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| Kept off the family tree | K012351 | FDA’s K012351 is Bdprobetec ET CT/GC Amplified Dna Assay Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree | 2001 |
| * | K012219 | Scalpfix Clip SystemSummary page 3…-Subject Device Predicate Device Predicate Device 510(k) Number TBD K012219 K123551 ClassificationI Procode 870.4450 / DXC 882.4150/ HBO 870.44… | 2001 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K140805 | Itclamp 50 | 2014 | 1 |
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?
- The line of descent spans 24 years and passes through 3 companies; a new generation was cleared every 12.2 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K140805 (Innovative Trauma Care, Inc., 2014) has gone furthest, with 1 descendant of its own.
- 1 other device also cites its predicate K012219.
How does its category compare?
All DXC devicesDXC Clamp, Vascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · DXC
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXC
215in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXC
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DXC
442in 2025
MAUDE reports naming product code DXC, 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 | 10 | 52 | 0 | 298 |
| 2008 | 3 | 29 | 2 | 302 |
| 2009 | 4 | 83 | 2 | 539 |
| 2010 | 2 | — | 1 | 600 |
| 2011 | 6 | 51 | 3 | 691 |
| 2012 | 5 | 73 | 0 | 548 |
| 2013 | 14 | 89 | 0 | 920 |
| 2014 | 4 | 157 | 1 | 494 |
| 2015 | 5 | 71 | 0 | 374 |
| 2016 | 3 | 91 | 0 | 494 |
| 2017 | 3 | 90 | 0 | 416 |
| 2018 | 2 | — | 0 | 391 |
| 2019 | 2 | — | 0 | 393 |
| 2020 | 3 | 209 | 0 | 404 |
| 2021 | 6 | 37 | 0 | 371 |
| 2022 | 1 | — | 1 | 273 |
| 2023 | 4 | 215 | 2 | 674 |
| 2024 | 1 | — | 0 | 375 |
| 2025 | 2 | — | 0 | 442 |
| 2026 | 4 | 125 | 0 | — |
What is it indicated for?
The iTClamp5O is a trauma clamp device for the temporary control of severe bleeding
in the extremities, axilla, inguinal areas and scalp.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K132651 · printed Nov 6, 2026
Cite this page
510(k) Report. “K132651: Itclamp 50.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132651
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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