510(k) · Cleared
ClearedTR Band
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Terumo Medical Corp. · DXC Clamp, Vascular
Cleared on Mar 28, 2007 after a 43-day review. The FDA summary names its predicate without a number. 24 later devices descend from it.
- Decided
- Mar 28, 2007
- Review
- 43 days
- Class
- Class II
- Product code
- DXC
- Recalls
- None
- Predicates
- 0
24 later devices descend from it, 11 citing it directly.
- This deviceK070423 TR BandTerumo Medical Corp. · 2007
- Descendant · cites it directly · 9 of its ownK092503 Radar Vascular Compression DevicesAdvanced Vascular Dynamics · 2009
- Descendant · cites it directly · 4 of its ownK152525 TR BAND Radial Compression DeviceTerumo Medical Corporation · 2015
- Descendant · cites it directly · 4 of its ownK111837 Radial Artery Compression TourniquetLepu Medical Technology (Beijing) Co., Ltd. · 2011
- Descendant · 2 generations on · 3 of its ownK142122 Radar Vascular Compression DeviceAdvanced Vascular Dynamics · 2014
- Descendant · 2 generations on · 3 of its ownK142359 Vasc Band hemostatLepu Medical Technology (Beijing) Co., Ltd. · 2014
Showing 5 of 24 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 24 · See all- K092503Radar Vascular Compression DevicesAdvanced Vascular Dynamics · 2009 · cites it directly9descendants
- K152525TR BAND Radial Compression DeviceTerumo Medical Corporation · 2015 · cites it directly4descendants
- K111837Radial Artery Compression TourniquetLepu Medical Technology (Beijing) Co., Ltd. · 2011 · cites it directly4descendants
- K142122Radar Vascular Compression DeviceAdvanced Vascular Dynamics · 2014 · 2 generations on3descendants
- K142359Vasc Band hemostatLepu Medical Technology (Beijing) Co., Ltd. · 2014 · 2 generations on3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K070423 | TR Band | Terumo Medical Corp. | 2007 | — |
| +1 | K092503 | Radar Vascular Compression Devices | Advanced Vascular Dynamics | 2009 | — |
| +1 | K152525 | TR BAND Radial Compression Device | Terumo Medical Corporation | 2015 | — |
| +1 | K111837 | Radial Artery Compression Tourniquet | Lepu Medical Technology (Beijing) Co., Ltd. | 2011 | — |
| +2 | K142122 | Radar Vascular Compression Device | Advanced Vascular Dynamics | 2014 | — |
| +2 | K142359 | Vasc Band hemostat | Lepu Medical Technology (Beijing) Co., Ltd. | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 3 | 0 |
| 2013 | 2 | 0 |
| 2014 | 3 | 0 |
| 2015 | 2 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 2 | 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? (1)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | Radstat Radial Artery Compression System Named without a submission number |
What descends from it? (24)
See all 2411 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K092503 | Radar Vascular Compression Devices | 2009 | 9 |
| K152525 | TR BAND Radial Compression Device | 2015 | 4 |
| K111837 | Radial Artery Compression Tourniquet | 2011 | 4 |
| K122405 | Air-Band Radial Compression Device | 2012 | 2 |
| K190318 | VASOBand Vascular Compression Device | 2019 | 1 |
| K162027 | TRAcelet Compression Device | 2016 | 1 |
| K151363 | Zephyr Vascular Compression Device | 2015 | 1 |
| K123041 | Vasostat Hemostasis Device | 2013 | 1 |
| K131411 | Coseal | 2013 | 0 |
| K123035 | Seal One | 2012 | 0 |
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, K092503 (Advanced Vascular Dynamics, 2009) has gone furthest, with 9 descendants of its own.
How does its category compare?
All DXC devicesDXC Clamp, Vascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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 TR BandTM is a compression device to assist hemostasis of the radial artery after a
transradial procedure.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K070423 · printed Nov 6, 2026
Cite this page
510(k) Report. “K070423: TR Band.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070423
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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