510(k) · Cleared
ClearedSureTouch Mobile Pressure Mapping System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sure, Inc. · NKA System, Documentation, Breast Lesion
Cleared on Jun 28, 2019 as substantially equivalent to DEN020001 (Assurance Medical, 2003) after a 368-day review. Its family tree reaches back 1 generation to 2003.
- Decided
- Jun 28, 2019
- Review
- 368 days
- Class
- Class II
- Product code
- NKA
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to DEN020001 (2003). No later device cites it as a predicate yet.
- Root · 1 generation backDEN020001 Breastview Visual Mapping SystemAssurance Medical · 2003
- This deviceK181672 SureTouch Mobile Pressure Mapping SystemSure, Inc. · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | DEN020001 | Breastview Visual Mapping System | Assurance Medical | 2003 | — |
| 0 (this device) | K181672 | SureTouch Mobile Pressure Mapping System | Sure, Inc. | 2019 | — |
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 NKA? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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 |
|---|---|---|---|
| * | DEN020001 | Breastview Visual Mapping SystemSummary page 4…Lesion Documentation System Product Code: NKA (System, Documentation, Breast Lesion) Regulatory Class: Class II Predicate Device: BreastView Visual Mapping System (DEN020001). This predicate device has not been subject to any design related recalls. Device Description: The SureTouch Mobile Pressure Ma… | 2003 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- Its one ancestor has no recall.
- 1 other device also cites its predicate DEN020001.
How does its category compare?
All NKA devicesNKA System, Documentation, Breast Lesion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · NKA
2in 2019
2026 to Oct 25, outlined.
Median 510(k) review, days · NKA
Too few NKA 510(k)s in any year since 2007 to give a median.
Recalls per year · NKA
No recall names NKA since 2007.
Adverse event reports per year · NKA
No MAUDE report names NKA since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 1 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The SureTouch Mobile Pressure Mapping System is intended to produce a surface pressure map of the breast as an aid in documenting palpable breast lesions identified during a clinical breast examination. The SureTouch Mobile Pressure Mapping System is intended for use by a qualified healthcare professional trained in its use and is not for home use.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K181672 · printed Nov 4, 2026
Cite this page
510(k) Report. “K181672: SureTouch Mobile Pressure Mapping System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K181672
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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