510(k) · Cleared
ClearedFriendship Medical Disposable Pre-Gelled AG / Agcl Surface Electrode
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Xian Friendship Medical Electronics Co., Ltd. · GXY Electrode, Cutaneous
Cleared on Aug 30, 2011 as substantially equivalent to K062198 (Axon Systems, Inc., 2006) and 1 other predicate after a 210-day review. Its family tree reaches back 2 generations to 1995. 2 later devices descend from it.
- Decided
- Aug 30, 2011
- Review
- 210 days
- Class
- Class II
- Product code
- GXY
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K941799 (1995). 5 ancestors in all, the oldest K821137 (1982). 2 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK941799 Disposable Cutaneous ElectrodesBio-Logic Systems Corp. · 1995
- 1 generation backK052188 Cutaneous ElectrodeRhythmlink International, LLC · 2005
- This deviceK110289 Friendship Medical Disposable Pre-Gelled AG / Agcl Surface ElectrodeXian Friendship Medical Electronics Co., Ltd. · 2011
- Descendant · cites it directly · 1 of its ownK142159 Disposable Pre-Gelled Surface ElectrodeRochester Electro Medical, Inc. · 2015
- Descendant · 2 generations on · 0 of its ownK172703 Disposable Snap ElectrodeEmbla Systems · 2017
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K941799 | Disposable Cutaneous Electrodes | Bio-Logic Systems Corp. | 1995 | — |
| −1 | K052188 | Cutaneous Electrode | Rhythmlink International, LLC | 2005 | — |
| 0 (this device) | K110289 | Friendship Medical Disposable Pre-Gelled AG / Agcl Surface Electrode | Xian Friendship Medical Electronics Co., Ltd. | 2011 | — |
| +1 | K142159 | Disposable Pre-Gelled Surface Electrode | Rochester Electro Medical, Inc. | 2015 | — |
| +2 | K172703 | Disposable Snap Electrode | Embla Systems | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1998 | 1 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 1 | 0 |
| 2017 | 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 GXY? 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 GXY device
- #1 K232052 Ceribell Instant EEG Headbandscore 16.3 · 6 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 |
|---|---|---|---|
| * | K062198 | Sunspots Pre-Gelled Surface ElectrodesSummary page 1…21 CFR section 882.1320. Cutaneous Electrode. Name: GXY Product Code: Predicate Devices: Sunspot Pre-gelled Surface Electrodes (K062198) manufactured by Axon Systems, Inc. Rthymlink International Cutaneous Pad… | 2006 |
| * | K052188 | Cutaneous ElectrodeSummary page 1…Surface Electrodes (K062198) manufactured by Axon Systems, Inc. Rthymlink International Cutaneous Pad Electrodes (K0521 88) manufactured by Rhythmlink International, LLC. 10.1 Device Description: Friendship's P… | 2005 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K142159 | Disposable Pre-Gelled Surface Electrode | 2015 | 1 |
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 3 companies; a new generation was cleared every 10.6 years on median.
- None of the 5 ancestors has a recall.
- Of its descendants, K142159 (Rochester Electro Medical, Inc., 2015) has gone furthest, with 1 descendant of its own.
- 2 other devices also cite its predicate K062198.
How does its category compare?
All GXY devicesGXY Electrode, Cutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · GXY
6in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GXY
148in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GXY
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GXY
58in 2025
MAUDE reports naming product code GXY, 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 | 7 | 88 | 0 | 14 |
| 2008 | 9 | 136 | 0 | 17 |
| 2009 | 17 | 159 | 4 | 15 |
| 2010 | 3 | 137 | 1 | 14 |
| 2011 | 6 | 183 | 5 | 16 |
| 2012 | 9 | 150 | 4 | 16 |
| 2013 | 7 | 99 | 0 | 15 |
| 2014 | 9 | 203 | 0 | 11 |
| 2015 | 6 | 119 | 0 | 19 |
| 2016 | 6 | 170 | 0 | 15 |
| 2017 | 9 | 116 | 0 | 11 |
| 2018 | 14 | 135 | 0 | 10 |
| 2019 | 9 | 113 | 0 | 19 |
| 2020 | 4 | 108 | 0 | 11 |
| 2021 | 12 | 195 | 0 | 21 |
| 2022 | 5 | 81 | 0 | 34 |
| 2023 | 13 | 132 | 2 | 25 |
| 2024 | 7 | 111 | 0 | 51 |
| 2025 | 6 | 148 | 0 | 58 |
| 2026 | 12 | 70 | 0 | — |
What is it indicated for?
Disposable Pre-gelled Ag/AgCI Surface Electrodes are intended for recording/stimulation and monitoring of the Electromygraphy (EMVG), Electroencephalograph(EEG) and Evoked Potential(EP) signals.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110289 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110289: Friendship Medical Disposable Pre-Gelled AG / Agcl Surface Electrode.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110289
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