510(k) · Cleared
ClearedElectrodes Handpieces for Mygen V-1000 RF System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
RF Medical Co., Ltd. · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Aug 3, 2020 as substantially equivalent to K180999 (RF Medical Co., Ltd., 2018) after a 243-day review. Its family tree reaches back 1 generation to 2018. 1 later device descends from it.
- Decided
- Aug 3, 2020
- Review
- 243 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K180999 (2018). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK180999 Mygen V-1000 RF SystemRF Medical Co., Ltd. · 2018
- This deviceK193355 Electrodes Handpieces for Mygen V-1000 RF SystemRF Medical Co., Ltd. · 2020
- Descendant · cites it directly · 0 of its ownK232763 Electrode Handpieces (VCT, RFTV, BMDT series)RF Medical Co., Ltd. · 2023
Most influential descendants
Showing 1 of 1 · See all- K232763Electrode Handpieces (VCT, RFTV, BMDT series)RF Medical Co., Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K180999 | Mygen V-1000 RF System | RF Medical Co., Ltd. | 2018 | — |
| 0 (this device) | K193355 | Electrodes Handpieces for Mygen V-1000 RF System | RF Medical Co., Ltd. | 2020 | — |
| +1 | K232763 | Electrode Handpieces (VCT, RFTV, BMDT series) | RF Medical Co., Ltd. | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2023 | 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? (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 |
|---|---|---|---|
| * | K180999 | Mygen V-1000 RF SystemSummary page 5…GEI, JOS Regulatory Class: Class II Prescription Use. 1 K193355 PREDICATE DEVICE (K180999) Primary Device Manufacturer: RF Medical Co. Ltd Trade/proprietary name: Electrodes Handpieces for Mygen V-1000 RF System Mo… | 2018 |
| † | K181249 | EUSRA RF Electrode | 2018 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K232763 | Electrode Handpieces (VCT, RFTV, BMDT series) | 2023 | 0 |
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?
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, 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?
Electrodes Handpieces (BT, JET) are indicated for coagulation and ablation of soft tissue when used in conjunction with
Mygen V-1000 radio frequency generator.
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/K193355 · printed Nov 4, 2026
Cite this page
510(k) Report. “K193355: Electrodes Handpieces for Mygen V-1000 RF System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K193355
Report an extraction error
Are you the manufacturer?
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