510(k) · Cleared
ClearedMyoSure MANUAL Tissue Removal Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hologic, Inc. · HIH Hysteroscope (And Accessories)
Cleared on May 8, 2018 as substantially equivalent to K142029 (Hologic, Inc., 2014) after a 137-day review. Its family tree reaches back 5 generations to 1995. 4 later devices descend from it.
- Decided
- May 8, 2018
- Review
- 137 days
- Class
- Class II
- Product code
- HIH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K953695 (1995). 9 ancestors in all. 4 later devices descend from it, 3 citing it directly.
- Root · 5 generations backK953695 Dyonics Disposable Arthroscopic BladesSmith & Nephew Dyonics, Inc. · 1995
- 4 generations backK031787 Smith & Nephew Iur Morcellation SystemSmith & Nephew, Inc. · 2003 · Recalled
- 3 generations backK041774 Iur Reciprocating Morcellator Model # 7210517Smith & Nephew, Inc. · 2004
- 2 generations backK132015 Truclear Morcellation System and Truclear MorcellatorsSmith & Nephew, Inc. · 2013 · Recalled
- 1 generation backK142029 Myosure Hysteroscopic Tissue Removal SystemHologic, Inc. · 2014
- This deviceK173901 MyoSure MANUAL Tissue Removal DeviceHologic, Inc. · 2018
- Descendant · cites it directly · 1 of its ownK191538 Resectr Tissue Resection DeviceBoston Scientific Corporation · 2020
- Descendant · 2 generations on · 0 of its ownK260984 HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device -…Axora Medical, Inc. · 2026
- Descendant · cites it directly · 0 of its ownK254050 Manual Tissue Removal DeviceSuzhou AcuVu Medical Technology Co., Ltd. · 2026
- Descendant · cites it directly · 0 of its ownK182675 Polygon Resection DevicePolygon Medical, Inc. · 2019
Most influential descendants
Showing 4 of 4 · See all- K191538Resectr Tissue Resection DeviceBoston Scientific Corporation · 2020 · cites it directly1descendant
- K260984HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device - 5 pack (5FR5PK)Axora Medical, Inc. · 2026 · 2 generations on0descendants
- K254050Manual Tissue Removal DeviceSuzhou AcuVu Medical Technology Co., Ltd. · 2026 · cites it directly0descendants
- K182675Polygon Resection DevicePolygon Medical, Inc. · 2019 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K953695 | Dyonics Disposable Arthroscopic Blades | Smith & Nephew Dyonics, Inc. | 1995 | — |
| −4 | K031787 | Smith & Nephew Iur Morcellation System | Smith & Nephew, Inc. | 2003 | 1 |
| −3 | K041774 | Iur Reciprocating Morcellator Model # 7210517 | Smith & Nephew, Inc. | 2004 | — |
| −2 | K132015 | Truclear Morcellation System and Truclear Morcellators | Smith & Nephew, Inc. | 2013 | 1 |
| −1 | K142029 | Myosure Hysteroscopic Tissue Removal System | Hologic, Inc. | 2014 | — |
| 0 (this device) | K173901 | MyoSure MANUAL Tissue Removal Device | Hologic, Inc. | 2018 | — |
| +1 | K191538 | Resectr Tissue Resection Device | Boston Scientific Corporation | 2020 | — |
| +2 | K260984 | HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device - 5 pack… | Axora Medical, Inc. | 2026 | — |
| +1 | K254050 | Manual Tissue Removal Device | Suzhou AcuVu Medical Technology Co., Ltd. | 2026 | — |
| +1 | K182675 | Polygon Resection Device | Polygon Medical, Inc. | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 1 | 0 |
| 1997 | 1 | 0 |
| 2011 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2019 | 1 | 0 |
| 2020 | 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 HIH? 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 HIH device
- #1 K232003 Endoscopic Video Image Processor, Single-Use…score 16.1 · 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? (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 |
|---|---|---|---|
| * | K142029 | Myosure Hysteroscopic Tissue Removal SystemSummary page 4…: Class II Panel: Obstetrics/Gynecology PREDICATE DEVICES Tradename: MyoSure LITE Tissue Removal Device Submitter/510(k) Holder: Hologic, Inc. 510(k) #: K142029 Product Code: HIH Regulation: 21.CFR.884.1690 The MyoSure LITE Tissue Removal Device has not been subject to a design-… | 2014 |
What descends from it? (4)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 23 years and passes through 3 companies; a new generation was cleared every 3.4 years on median.
- 2 of the 9 ancestors have a recall of any class.
- Of its descendants, K191538 (Boston Scientific Corporation, 2020) has gone furthest, with 1 descendant of its own.
- 2 other devices also cite its predicate K142029.
How does its category compare?
All HIH devicesHIH Hysteroscope (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.
FDA decisions per year · HIH
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HIH
111in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HIH
3so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HIH
1,698in 2025
MAUDE reports naming product code HIH, 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 | 1 | — | 0 | 7 |
| 2008 | 2 | — | 0 | 12 |
| 2009 | 4 | 130 | 0 | 17 |
| 2010 | 4 | 109 | 0 | 31 |
| 2011 | 3 | 118 | 0 | 59 |
| 2012 | 4 | 25 | 0 | 78 |
| 2013 | 5 | 144 | 0 | 111 |
| 2014 | 2 | — | 0 | 125 |
| 2015 | 5 | 52 | 0 | 211 |
| 2016 | 3 | 106 | 0 | 172 |
| 2017 | 2 | — | 0 | 336 |
| 2018 | 8 | 135 | 0 | 182 |
| 2019 | 14 | 91 | 1 | 220 |
| 2020 | 7 | 88 | 0 | 253 |
| 2021 | 4 | 194 | 0 | 193 |
| 2022 | 2 | — | 0 | 289 |
| 2023 | 4 | 200 | 2 | 1,449 |
| 2024 | 6 | 148 | 0 | 1,611 |
| 2025 | 3 | 111 | 0 | 1,698 |
| 2026 | 7 | 168 | 3 | — |
What is it indicated for?
The MyoSure MANUAL Tissue Removal Device is intended for intrauterine use by a trained gynecologist to
hysteroscopically resect and remove tissue, including focal lesions such as endometrial polyps and retained products of
conception.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K173901 · printed Nov 6, 2026
Cite this page
510(k) Report. “K173901: MyoSure MANUAL Tissue Removal Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173901
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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