510(k) · Cleared
ClearedDomain Surgical System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Domain Surgical, Inc. · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Jul 18, 2011 as substantially equivalent to K091107 (Hemostatix Medical Technologies, LLC, 2009) and 1 other predicate after a 153-day review. Its family tree reaches back 2 generations to 2004. 5 later devices descend from it.
- Decided
- Jul 18, 2011
- Review
- 153 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K033089 (2004). 3 ancestors in all, the oldest K844403 (1985). 5 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK033089 Hemostatix, Model 2400Z Thermal Scalpel SystemGyrus Ent LLC · 2004 · Recalled
- 1 generation backK091107 Model P8400 Hemostatix Thermal Scalpel SystemHemostatix Medical Technologies, LLC · 2009 · Recalled
- This deviceK110439 Domain Surgical SystemDomain Surgical, Inc. · 2011
- Descendant · cites it directly · 4 of its ownK121881 Domain Surgical SystemDomain Surgical, Inc. · 2012
- Descendant · 2 generations on · 3 of its ownK130606 Fmwand Ferromagnetic Surgical SystemDomain Surgical, Inc. · 2014
- Descendant · 3 generations on · 1 of its ownK141484 Open FmsealerDomain Surgical, Inc. · 2014 · Recalled
- Descendant · 4 generations on · 0 of its ownK142229 Laparoscopic FMsealerDomain Surgical, Inc. · 2015
- Descendant · 3 generations on · 0 of its ownK140384 Fmwand Handpiece SEDomain Surgical, Inc. · 2014
Most influential descendants
Showing 5 of 5 · See all- K121881Domain Surgical SystemDomain Surgical, Inc. · 2012 · cites it directly4descendants
- K130606Fmwand Ferromagnetic Surgical SystemDomain Surgical, Inc. · 2014 · 2 generations on3descendants
- K141484Open FmsealerDomain Surgical, Inc. · 2014 · 3 generations on1descendant
- K142229Laparoscopic FMsealerDomain Surgical, Inc. · 2015 · 4 generations on0descendants
- K140384Fmwand Handpiece SEDomain Surgical, Inc. · 2014 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K033089 | Hemostatix, Model 2400Z Thermal Scalpel System | Gyrus Ent LLC | 2004 | 2 |
| −1 | K091107 | Model P8400 Hemostatix Thermal Scalpel System | Hemostatix Medical Technologies, LLC | 2009 | 2 |
| 0 (this device) | K110439 | Domain Surgical System | Domain Surgical, Inc. | 2011 | — |
| +1 | K121881 | Domain Surgical System | Domain Surgical, Inc. | 2012 | — |
| +2 | K130606 | Fmwand Ferromagnetic Surgical System | Domain Surgical, Inc. | 2014 | — |
| +3 | K141484 | Open Fmsealer | Domain Surgical, Inc. | 2014 | 1 |
| +4 | K142229 | Laparoscopic FMsealer | Domain Surgical, Inc. | 2015 | — |
| +3 | K140384 | Fmwand Handpiece SE | Domain Surgical, Inc. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1985 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2014 | 3 | 0 |
| 2015 | 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 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? (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 |
|---|---|---|---|
| * | K091107 | Model P8400 Hemostatix Thermal Scalpel SystemSummary page 1…ce and accessories Name of Predicate Device(s) * Hemostatix Medical Technologies, LLC - Model P8400 Hemostatix Thermal Scaipel System, (Product Code GEl) 510(k) #K091107 * Valleylab Force 2 Electrosurgical Generator (Product Code GEl) 510(k) #K844403 Device Description An electrosurgical c… | 2009 |
| * | K844403 | Model Force 2 Electrosurgical GeneratorSummary page 1…LLC - Model P8400 Hemostatix Thermal Scaipel System, (Product Code GEl) 510(k) #K091107 * Valleylab Force 2 Electrosurgical Generator (Product Code GEl) 510(k) #K844403 Device Description An electrosurgical cutting and coagulation device (and accessories) is a device intended to remov… | 1985 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K121881 | Domain Surgical System | 2012 | 4 |
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 7 years and passes through 3 companies; a new generation was cleared every 5.2 years on median.
- 2 of the 3 ancestors have a recall of any class.
- Of its descendants, K121881 (Domain Surgical, Inc., 2012) has gone furthest, with 4 descendants of its own.
- 2 other devices also cite its predicate K091107.
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?
The Domain Surgical System is indicated for cutting and coagulation of soft tissue.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110439 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110439: Domain Surgical System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110439
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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