510(k) · Cleared
ClearedFractora
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Invasix, Ltd. · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Jun 2, 2011 as substantially equivalent to K073572 (Syneron Medical, Ltd., 2008) after a 279-day review. Its family tree reaches back 16 generations to 1995. 24 later devices descend from it.
- Decided
- Jun 2, 2011
- Review
- 279 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 16 generations to K943450 (1995). 224 ancestors in all, the oldest K800617 (1980). 24 later devices descend from it, 4 citing it directly.
- Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 12 generations between
- 3 generations backK071786 Portrait PSRRhytec Incorporated · 2007
- 2 generations backK072394 Portrait Stand-OffRhytec Incorporated · 2007
- 1 generation backK073572 Matrix RF ApplicatorSyneron Medical, Ltd. · 2008
- This deviceK102461 FractoraInvasix, Ltd. · 2011
- Descendant · cites it directly · 9 of its ownK150161 Venus Viva SR DeviceVenus Concept, Ltd. · 2015
- Descendant · cites it directly · 5 of its ownK131758 Surgen UPollogen, Ltd. · 2013
- Descendant · cites it directly · 4 of its ownK203299 CellFX SystemPulse Biosciences, Inc. · 2021
- Descendant · 2 generations on · 4 of its ownK171359 Pollogen Legend+ SystemPollogen, Ltd. · 2017
- Descendant · 2 generations on · 3 of its ownK211444 CellFX SystemPulse Biosciences, Inc. · 2021
Show all 16 generations
- Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 15 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
- 14 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
- 13 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
- 12 generations backK973478 Arthrocare Sinus Electrosurgery SystemArthrocare Corp. · 1998
- 11 generations backK981870 Visage Cosmetic Surgery SystemArthrocare Corp. · 1998
- 10 generations backK000944 Thermage Thermacool SystemThermage, Inc. · 2000
- 9 generations backK013034 Modification to: Thermacool IiaThermage, Inc. · 2001
- 8 generations backK013639 Thermage Thermacool TC SystemThermage, Inc. · 2002
- 7 generations backK021402 Thermage Thermacool TC SystemThermage, Inc. · 2002
- 6 generations backK032088 Modification to Thermacool TC SystemThermage, Inc. · 2003
- 5 generations backK052778 Thermage Thermacool Skin MarketingThermage, Inc. · 2005
- 4 generations backK060948 Portrait PSR3Rhytec Incorporated · 2006 · Recalled
- 3 generations backK071786 Portrait PSRRhytec Incorporated · 2007
- 2 generations backK072394 Portrait Stand-OffRhytec Incorporated · 2007
- 1 generation backK073572 Matrix RF ApplicatorSyneron Medical, Ltd. · 2008
- This deviceK102461 FractoraInvasix, Ltd. · 2011
Showing 5 of 24 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 24 · See all- K150161Venus Viva SR DeviceVenus Concept, Ltd. · 2015 · cites it directly9descendants
- K131758Surgen UPollogen, Ltd. · 2013 · cites it directly5descendants
- K203299CellFX SystemPulse Biosciences, Inc. · 2021 · cites it directly4descendants
- K171359Pollogen Legend+ SystemPollogen, Ltd. · 2017 · 2 generations on4descendants
- K211444CellFX SystemPulse Biosciences, Inc. · 2021 · 2 generations on3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −16 | K943450 | Arthrocare Arthroscopic Electrosurgery System Model 970 | Arthrocare Corp. | 1995 | — |
| −15 | K961069 | Arthrocare Urologic Multi-Electrode Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −14 | K962445 | Arthrocare Dental Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −13 | K964849 | Arthrocare Dermatologic Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −12 | K973478 | Arthrocare Sinus Electrosurgery System | Arthrocare Corp. | 1998 | — |
| −11 | K981870 | Visage Cosmetic Surgery System | Arthrocare Corp. | 1998 | — |
| −10 | K000944 | Thermage Thermacool System | Thermage, Inc. | 2000 | — |
| −9 | K013034 | Modification to: Thermacool Iia | Thermage, Inc. | 2001 | — |
| −8 | K013639 | Thermage Thermacool TC System | Thermage, Inc. | 2002 | — |
| −7 | K021402 | Thermage Thermacool TC System | Thermage, Inc. | 2002 | — |
| −6 | K032088 | Modification to Thermacool TC System | Thermage, Inc. | 2003 | — |
| −5 | K052778 | Thermage Thermacool Skin Marketing | Thermage, Inc. | 2005 | — |
| −4 | K060948 | Portrait PSR3 | Rhytec Incorporated | 2006 | 1 |
| −3 | K071786 | Portrait PSR | Rhytec Incorporated | 2007 | — |
| −2 | K072394 | Portrait Stand-Off | Rhytec Incorporated | 2007 | — |
| −1 | K073572 | Matrix RF Applicator | Syneron Medical, Ltd. | 2008 | — |
| 0 (this device) | K102461 | Fractora | Invasix, Ltd. | 2011 | — |
| +1 | K150161 | Venus Viva SR Device | Venus Concept, Ltd. | 2015 | — |
| +1 | K131758 | Surgen U | Pollogen, Ltd. | 2013 | — |
| +1 | K203299 | CellFX System | Pulse Biosciences, Inc. | 2021 | — |
| +2 | K171359 | Pollogen Legend+ System | Pollogen, Ltd. | 2017 | — |
| +2 | K211444 | CellFX System | Pulse Biosciences, Inc. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1980 | 1 | 0 |
| 1982 | 2 | 0 |
| 1986 | 1 | 0 |
| 1988 | 2 | 0 |
| 1989 | 1 | 0 |
| 1990 | 2 | 0 |
| 1991 | 5 | 0 |
| 1992 | 3 | 0 |
| 1993 | 8 | 0 |
| 1994 | 15 | 0 |
| 1995 | 13 | 0 |
| 1996 | 18 | 0 |
| 1997 | 14 | 0 |
| 1998 | 12 | 0 |
| 1999 | 10 | 0 |
| 2000 | 19 | 0 |
| 2001 | 20 | 0 |
| 2002 | 25 | 0 |
| 2003 | 20 | 0 |
| 2004 | 10 | 0 |
| 2005 | 4 | 0 |
| 2006 | 1 | 0 |
| 2007 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 4 | 0 |
| 2022 | 5 | 0 |
| 2023 | 2 | 0 |
| 2024 | 1 | 0 |
| 2025 | 5 | 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 GEI? 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 GEI device
- #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 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 |
|---|---|---|---|
| * | K073572 | Matrix RF ApplicatorSummary page 1…gical Cutting and Coagulation and Accessories (21CFR §878.4400) Product code: GEL Predicate device Matrix RF applicator (K073572). Intended use: The Fractora is intended for dermatological procedures requiring ablation and resurfacing of the skin. Device… | 2008 |
What descends from it? (24)
See all 244 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 16 years and passes through 5 companies; a new generation was cleared every 11 months on median.
- 10 of the 224 ancestors have a recall of any class.
- Of its descendants, K150161 (Venus Concept, Ltd., 2015) has gone furthest, with 9 descendants of its own.
- 4 other devices also cite its predicate K073572.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · GEI
52in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEI
113in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEI
4in 2025
Class I (14 since 2007) Class II/III not classified
Adverse event reports per year · GEI
7,592in 2025
MAUDE reports naming product code GEI, 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 | 50 | 51 | 21 | 2,795 |
| 2008 | 61 | 71 | 19 | 2,556 |
| 2009 | 42 | 130 | 27 | 3,591 |
| 2010 | 46 | 109 | 51 | 3,377 |
| 2011 | 35 | 135 | 32 | 4,463 |
| 2012 | 39 | 133 | 30 | 5,216 |
| 2013 | 48 | 136 | 13 | 4,897 |
| 2014 | 49 | 103 | 3 | 4,908 |
| 2015 | 47 | 123 | 4 | 4,936 |
| 2016 | 64 | 108 | 3 | 5,616 |
| 2017 | 52 | 72 | 2 | 6,073 |
| 2018 | 47 | 93 | 6 | 6,545 |
| 2019 | 48 | 93 | 5 | 7,067 |
| 2020 | 59 | 105 | 1 | 6,490 |
| 2021 | 46 | 146 | 6 | 6,354 |
| 2022 | 55 | 150 | 49 | 6,103 |
| 2023 | 65 | 104 | 27 (4) | 7,176 |
| 2024 | 59 | 125 | 22 (10) | 7,897 |
| 2025 | 52 | 113 | 4 | 7,592 |
| 2026 | 43 | 183 | 8 | — |
What is it indicated for?
Fractora is intended for dermatological procedures requiring ablation and resurfacing of the skin.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102461 · printed Nov 3, 2026
Cite this page
510(k) Report. “K102461: Fractora.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K102461
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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