510(k) · Cleared
ClearedBemitt, Model 0001
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dja Distributors, LLC · IZH System, X-Ray, Mammographic
Cleared on Oct 26, 2007 as substantially equivalent to K023390 (Mbf Sales, LLC, 2002) and 1 other predicate after a 116-day review. Its family tree reaches back 5 generations to 1995.
- Decided
- Oct 26, 2007
- Review
- 116 days
- Class
- Class II
- Product code
- IZH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K955249 (1995). No later device cites it as a predicate yet.
- Root · 5 generations backK955249 Sensor PadInventive Products, Inc. · 1995
- 4 generations backK973450 Sensor PadInventive Products, Inc. · 1997
- 3 generations backK991469 Aware PadAac Consulting Group, Inc. · 1999
- 2 generations backK023390 MY Breast Friend, Breast Self-Exam PadMbf Sales, LLC · 2002
- 1 generation backK042250 SensatouchAluna Management Co., Ltd. · 2004
- This deviceK071787 Bemitt, Model 0001Dja Distributors, LLC · 2007
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K955249 | Sensor Pad | Inventive Products, Inc. | 1995 | — |
| −4 | K973450 | Sensor Pad | Inventive Products, Inc. | 1997 | — |
| −3 | K991469 | Aware Pad | Aac Consulting Group, Inc. | 1999 | — |
| −2 | K023390 | MY Breast Friend, Breast Self-Exam Pad | Mbf Sales, LLC | 2002 | — |
| −1 | K042250 | Sensatouch | Aluna Management Co., Ltd. | 2004 | — |
| 0 (this device) | K071787 | Bemitt, Model 0001 | Dja Distributors, LLC | 2007 | — |
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 IZH? 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 IZH device
- #1 K202294 Affirm Contrast Biopsyscore 1.0 · 4 generations · no Class I recall
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K023390 | MY Breast Friend, Breast Self-Exam PadSummary page 1…substantially equivalent to the previously cleared My Breast Friend device from MBF Sales, LLC (Rock-ville, MD). The predicate 510(k) number is K023390, and Sensa Touch Breast Self Exam Glove from Sante Feminine LTD (Smyrna, Ga). The predicate 5 10(k) is K(04225 0. BeM… | 2002 |
| * | K042250 | Sensatouch | 2004 |
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?
- The line of descent spans 12 years and passes through 5 companies; a new generation was cleared every 2.0 years on median.
- None of the 5 ancestors has a recall.
- 3 other devices also cite its predicate K023390.
How does its category compare?
All IZH devicesIZH System, X-Ray, Mammographic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · IZH
1in 2021
2026 to Oct 25, outlined.
Median 510(k) review, days · IZH
64in 2016
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IZH
2in 2008
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IZH
15in 2025
MAUDE reports naming product code IZH, 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 | 3 | 30 | 0 | 11 |
| 2008 | 1 | — | 2 | 5 |
| 2009 | 0 | — | 0 | 14 |
| 2010 | 2 | — | 0 | 7 |
| 2011 | 1 | — | 0 | 5 |
| 2012 | 2 | — | 0 | 18 |
| 2013 | 2 | — | 0 | 9 |
| 2014 | 0 | — | 0 | 7 |
| 2015 | 1 | — | 0 | 8 |
| 2016 | 3 | 64 | 0 | 9 |
| 2017 | 0 | — | 0 | 12 |
| 2018 | 0 | — | 0 | 25 |
| 2019 | 1 | — | 0 | 39 |
| 2020 | 1 | — | 0 | 7 |
| 2021 | 1 | — | 0 | 9 |
| 2022 | 0 | — | 0 | 4 |
| 2023 | 0 | — | 0 | 8 |
| 2024 | 0 | — | 0 | 5 |
| 2025 | 0 | — | 0 | 15 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The BeMittTM Self Breast Exam is indicated as an aid for performing breast-self examinations.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K071787 · printed Nov 4, 2026
Cite this page
510(k) Report. “K071787: Bemitt, Model 0001.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071787
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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