510(k) · Cleared
Recalled · Class II · 2017GID 700
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
The Gid Group, Inc. · MUU System, Suction, Lipoplasty
Cleared on Aug 15, 2012 as substantially equivalent to K092482 (Shippert Medical Technologies Corp., 2009) after a 142-day review. Its family tree reaches back 7 generations to 1991. 11 later devices descend from it. It has been recalled once.
- Decided
- Aug 15, 2012
- Review
- 142 days
- Class
- Class II
- Product code
- MUU
- Recalls
- 1
- Predicates
- 1
Its longest line of descent runs back 7 generations to K910696 (1991). 27 ancestors in all, the oldest K861153 (1986). 11 later devices descend from it, 5 citing it directly.
- Root · 7 generations backK910696 Cusa (R) System 200C/200T/200M/200H Ultra AspiratorValleylab, Inc. · 1991
- 6 generations backK970471 Mentor Ultrasound Assisted Tissue Removal System (TRS)Mentor Corp. · 1997
- 5 generations backK983065 Mentor Ultrasound-Assisted Tissue Removal SystemMentor Corp. · 1998
- 4 generations backK022051 Soundvaser SystemSound Surgical Technologies, LLC · 2002 · Recalled
- 3 generations backK042261 Macropore Puricel Lipoplasty SystemMacropore Biosurgery, Inc. · 2004
- 2 generations backK072587 Cytori Aft SystemCytori Therapeutics, Inc. · 2007
- 1 generation backK092482 Tissu Trans Filtron, Models 3-TT-Filtron 2000-500Shippert Medical Technologies Corp. · 2009 · Recalled
- This deviceK120902 GID 700The Gid Group, Inc. · 2012
- Descendant · cites it directly · 6 of its ownK142682 The Lipogems SystemLipogems International Spa · 2014
- Descendant · 2 generations on · 5 of its ownK161636 Lipogems SystemLipogems International Spa · 2016
- Descendant · 3 generations on · 2 of its ownK171135 Lipogems SystemLipogems International Spa · 2017
- Descendant · 4 generations on · 1 of its ownK193363 Dermapose RefreshPuregraft, LLC · 2020
- Descendant · 3 generations on · 0 of its ownK210528 IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit…Millennium Medical Technologies Inc (Dba Cellmyx) · 2022
Showing 5 of 11 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 11 · See all- K142682The Lipogems SystemLipogems International Spa · 2014 · cites it directly6descendants
- K161636Lipogems SystemLipogems International Spa · 2016 · 2 generations on5descendants
- K171135Lipogems SystemLipogems International Spa · 2017 · 3 generations on2descendants
- K193363Dermapose RefreshPuregraft, LLC · 2020 · 4 generations on1descendant
- K210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On…Millennium Medical Technologies Inc (Dba Cellmyx) · 2022 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K910696 | Cusa (R) System 200C/200T/200M/200H Ultra Aspirator | Valleylab, Inc. | 1991 | — |
| −6 | K970471 | Mentor Ultrasound Assisted Tissue Removal System (TRS) | Mentor Corp. | 1997 | — |
| −5 | K983065 | Mentor Ultrasound-Assisted Tissue Removal System | Mentor Corp. | 1998 | — |
| −4 | K022051 | Soundvaser System | Sound Surgical Technologies, LLC | 2002 | 2 |
| −3 | K042261 | Macropore Puricel Lipoplasty System | Macropore Biosurgery, Inc. | 2004 | — |
| −2 | K072587 | Cytori Aft System | Cytori Therapeutics, Inc. | 2007 | — |
| −1 | K092482 | Tissu Trans Filtron, Models 3-TT-Filtron 2000-500 | Shippert Medical Technologies Corp. | 2009 | 8 |
| 0 (this device) | K120902 | GID 700 | The Gid Group, Inc. | 2012 | — |
| +1 | K142682 | The Lipogems System | Lipogems International Spa | 2014 | — |
| +2 | K161636 | Lipogems System | Lipogems International Spa | 2016 | — |
| +3 | K171135 | Lipogems System | Lipogems International Spa | 2017 | — |
| +4 | K193363 | Dermapose Refresh | Puregraft, LLC | 2020 | — |
| +3 | K210528 | IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat… | Millennium Medical Technologies Inc (Dba Cellmyx) | 2022 | — |
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 |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 3 | 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? (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 |
|---|---|---|---|
| * | K092482 | Tissu Trans Filtron, Models 3-TT-Filtron 2000-500Summary page 2…The OlD 700 is Substantially equivalent to the Shippert Tissu- Trans Filtron 1000 canister (K092482) manufactured by Shippert Medical based on design, materials, and testing.… | 2009 |
What descends from it? (11)
See all 115 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 |
|---|---|---|---|---|
| Aug 8, 2017 | Class II | Z-0823-2018 | Material/Component Contamination | Presence of bacterial endotoxins levels above the acceptable limit |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 21 years and passes through 7 companies; a new generation was cleared every 2.7 years on median.
- 5 of the 27 ancestors have a recall of any class.
- Of its descendants, K142682 (Lipogems International Spa, 2014) has gone furthest, with 6 descendants of its own.
- 3 other devices also cite its predicate K092482.
How does its category compare?
All MUU devicesMUU System, Suction, Lipoplasty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, 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 GID 700 is used for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring. The system should be used with a legally marketed vacuum or aspirator apparatus as a source of suction. If harvested fat is to be reimplanted, the harvested fat is only to be used without any additional manipulation.
The GID 700 is intended for use in the following surgical specialties when aspiration of soft tissue is desired: plastic and reconstructive surgery, neurosurgery, gastrointestinal and affiliated organ surgery, urological surgery, general surgery, orthopedic surgery, gynecological surgery, thoracic surgery, and laparoscopic surgery.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K120902 · printed Nov 6, 2026
Cite this page
510(k) Report. “K120902: GID 700.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K120902
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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