510(k) · Cleared
Recalled · Class II · 2018Tissu Trans Filtron, Models 3-TT-Filtron 2000-500
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shippert Medical Technologies Corp. · MUU System, Suction, Lipoplasty
Cleared on Dec 4, 2009 as substantially equivalent to K072587 (Cytori Therapeutics, Inc., 2007) and 1 other predicate after a 113-day review. Its family tree reaches back 6 generations to 1991. 17 later devices descend from it. It has been recalled 8 times.
- Decided
- Dec 4, 2009
- Review
- 113 days
- Class
- Class II
- Product code
- MUU
- Recalls
- 8
- Predicates
- 2
Its longest line of descent runs back 6 generations to K910696 (1991). 26 ancestors in all, the oldest K861153 (1986). 17 later devices descend from it, 4 citing it directly.
- Root · 6 generations backK910696 Cusa (R) System 200C/200T/200M/200H Ultra AspiratorValleylab, Inc. · 1991
- 5 generations backK970471 Mentor Ultrasound Assisted Tissue Removal System (TRS)Mentor Corp. · 1997
- 4 generations backK983065 Mentor Ultrasound-Assisted Tissue Removal SystemMentor Corp. · 1998
- 3 generations backK022051 Soundvaser SystemSound Surgical Technologies, LLC · 2002 · Recalled
- 2 generations backK042261 Macropore Puricel Lipoplasty SystemMacropore Biosurgery, Inc. · 2004
- 1 generation backK072587 Cytori Aft SystemCytori Therapeutics, Inc. · 2007
- This deviceK092482 Tissu Trans Filtron, Models 3-TT-Filtron 2000-500Shippert Medical Technologies Corp. · 2009
- Descendant · cites it directly · 11 of its ownK120902 GID 700The Gid Group, Inc. · 2012 · Recalled
- Descendant · 2 generations on · 6 of its ownK142682 The Lipogems SystemLipogems International Spa · 2014
- Descendant · 3 generations on · 5 of its ownK161636 Lipogems SystemLipogems International Spa · 2016
- Descendant · 4 generations on · 2 of its ownK171135 Lipogems SystemLipogems International Spa · 2017
- Descendant · cites it directly · 2 of its ownK120328 Origins Lipoharvesting SystemSound Surgical Technologies, LLC · 2012
Showing 5 of 17 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 17 · See all- K120902GID 700The Gid Group, Inc. · 2012 · cites it directly11descendants
- K142682The Lipogems SystemLipogems International Spa · 2014 · 2 generations on6descendants
- K161636Lipogems SystemLipogems International Spa · 2016 · 3 generations on5descendants
- K171135Lipogems SystemLipogems International Spa · 2017 · 4 generations on2descendants
- K120328Origins Lipoharvesting SystemSound Surgical Technologies, LLC · 2012 · cites it directly2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K910696 | Cusa (R) System 200C/200T/200M/200H Ultra Aspirator | Valleylab, Inc. | 1991 | — |
| −5 | K970471 | Mentor Ultrasound Assisted Tissue Removal System (TRS) | Mentor Corp. | 1997 | — |
| −4 | K983065 | Mentor Ultrasound-Assisted Tissue Removal System | Mentor Corp. | 1998 | — |
| −3 | K022051 | Soundvaser System | Sound Surgical Technologies, LLC | 2002 | 2 |
| −2 | K042261 | Macropore Puricel Lipoplasty System | Macropore Biosurgery, Inc. | 2004 | — |
| −1 | K072587 | Cytori Aft System | Cytori Therapeutics, Inc. | 2007 | — |
| 0 (this device) | K092482 | Tissu Trans Filtron, Models 3-TT-Filtron 2000-500 | Shippert Medical Technologies Corp. | 2009 | — |
| +1 | K120902 | GID 700 | The Gid Group, Inc. | 2012 | 1 |
| +2 | K142682 | The Lipogems System | Lipogems International Spa | 2014 | — |
| +3 | K161636 | Lipogems System | Lipogems International Spa | 2016 | — |
| +4 | K171135 | Lipogems System | Lipogems International Spa | 2017 | — |
| +1 | K120328 | Origins Lipoharvesting System | Sound Surgical Technologies, LLC | 2012 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1986 | 2 | 0 |
| 1988 | 2 | 0 |
| 1992 | 1 | 0 |
| 1994 | 1 | 0 |
| 1995 | 2 | 0 |
| 1996 | 2 | 0 |
| 1997 | 2 | 0 |
| 1998 | 3 | 0 |
| 1999 | 3 | 0 |
| 2001 | 1 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
| 2012 | 2 | 0 |
| 2014 | 1 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 5 | 0 |
| 2019 | 2 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2022 | 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 MUU? 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 MUU device
- #1 K210528 IntelliFat Disposable Adipose Tissue…score 5.7 · 10 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K072587 | Cytori Aft SystemSummary page 4…external sources of vacuum to withdraw, hold, and/or inject fluids/tissues into the body. The Tissu Trans Filtron is substantially equivalent to the Cytori AFT System k072587, The Shippert Medical Tissu Trans k<050797 and the Lipivage k# unknown, predicate devices as they all consist of a polycarbonate… | 2007 |
| * | K050797 | Tissu-TransSummary page 3…inciples with the following predicate devices,, c~aebeen determined byfFPA~to~bgsubstantiaIly equivalent to premar-ket devices: Cytari AFT,Systenr k 7257 l rn k050797, and Genesis Biasystems Lipivage (510(ky,number unknown); Class I and Class II medica!.devlces that were cleared for marketing in… | 2005 |
| * | — | Genesis Biosystems Lipivage Named without a submission number |
What descends from it? (17)
See all 174 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)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 2, 2018 | Class II | Z-1330-2019 | Packaging process control | The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch. |
| Feb 2, 2018 | Class II | Z-1331-2019 | Packaging process control | The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch. |
| Feb 2, 2018 | Class II | Z-1333-2019 | Packaging process control | |
| Feb 2, 2018 | Class II | Z-1332-2019 | Packaging process control | The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch. |
| Feb 2, 2018 | Class II | Z-1335-2019 | Packaging process control | The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch. |
| Feb 2, 2018 | Class II | Z-1336-2019 | Packaging process control | The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch. |
| Feb 2, 2018 | Class II | Z-1334-2019 | Packaging process control | |
| Oct 20, 2017 | Class II | Z-0170-2018 | Packaging process control | Potential breach of sterility of the packaging. |
The 5 latest of 8 recalls; the web page lists all.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 18 years and passes through 6 companies; a new generation was cleared every 3.2 years on median.
- 4 of the 26 ancestors have a recall of any class.
- Of its descendants, K120902 (The Gid Group, Inc., 2012) has gone furthest, with 11 descendants of its own.
- 5 other devices also cite its predicate K072587.
How does its category compare?
All MUU devicesMUU System, Suction, Lipoplasty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.
FDA decisions per year · MUU
1in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · MUU
190in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MUU
2in 2017
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MUU
10in 2025
MAUDE reports naming product code MUU, 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 | — | 1 | 2 |
| 2008 | 1 | — | 0 | 4 |
| 2009 | 3 | 113 | 0 | 2 |
| 2010 | 4 | 58 | 0 | 4 |
| 2011 | 0 | — | 0 | 5 |
| 2012 | 5 | 171 | 0 | 4 |
| 2013 | 1 | — | 0 | 21 |
| 2014 | 4 | 114 | 0 | 13 |
| 2015 | 3 | 269 | 1 | 44 |
| 2016 | 1 | — | 1 | 20 |
| 2017 | 7 | 91 | 2 | 28 |
| 2018 | 1 | — | 0 | 30 |
| 2019 | 4 | 190 | 0 | 35 |
| 2020 | 2 | — | 0 | 36 |
| 2021 | 2 | — | 0 | 28 |
| 2022 | 1 | — | 0 | 50 |
| 2023 | 0 | — | 0 | 15 |
| 2024 | 0 | — | 0 | 5 |
| 2025 | 0 | — | 0 | 10 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Tissu Trans Filtron is intended to be used with house vacuum and/or cleared pumps, tubing and cannulas, for the collection of aspirated fat, for aesthetic body contouring. If the fat is untreated, it may be reinjected via a cleared injection apparatus.
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/K092482 · printed Nov 4, 2026
Cite this page
510(k) Report. “K092482: Tissu Trans Filtron, Models 3-TT-Filtron 2000-500.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K092482
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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