Devices › Electrosurgical, cutting & coagulation & accessories
Device brand name · Electrosurgical dispersive electrode
Skintact: medical device reports filed with FDA
245 reports name it, 2007–2026. Product code GEI.
- 245
- device reports naming the brand
- 0% of all MAUDE reports · about 13 a year
- 17
- reports, 12 months to August 2026
- 13 in the 12 months before
- 24.5%
- classified as malfunction
- 80.1% across the product code
- 0.4%
- classified as death, as reported
- 1 reports · not verified by FDA
245 medical device reports received by FDA name the brand "Skintact" (electrosurgical dispersive electrode); received from June 2007 to July 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
17 reports arrived in the 12 months to August 2026, up 31% from 13 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (75.1%), malfunction (24.5%) and death (0.4%); across all electrosurgical, cutting & coagulation & accessories reports (product code GEI) death is recorded in 0.4% and malfunction in 80.1%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are insufficient device problem information (52.2%), fitting problem (3.3%) and defective device (2%). The patient problems coded most often are burn(s), skin irritation and skin tears. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 118,290 reports carrying product code GEI. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Insufficient device problem information | 128 | 52.2% | 2.8% |
| Fitting problem | 8 | 3.3% | 0.2% |
| Defective devicethe device was defective | 5 | 2% | 0.6% |
| Device handling problem | 5 | 2% | 0% |
| Electrical /electronic property probleman electrical or electronic problem | 4 | 1.6% | 2.7% |
| No display/image | 4 | 1.6% | 0.1% |
| Patient device interaction problem | 4 | 1.6% | 0.2% |
| Device operates differently than expectedthe device behaved unexpectedly | 3 | 1.2% | 3.9% |
| Device sensing problem | 3 | 1.2% | 0% |
| Mechanical problema mechanical problem | 3 | 1.2% | 1.2% |
| Connection problema connection problem | 2 | 0.8% | 0.7% |
| Missing information | 2 | 0.8% | 0% |
| Overheating of device | 2 | 0.8% | 1.3% |
| Compatibility problem | 1 | 0.4% | 0% |
| Data problem | 1 | 0.4% | 0% |
| Defective component | 1 | 0.4% | 0.3% |
| Defibrillation/stimulation problem | 1 | 0.4% | 0% |
| Detachment of device component | 1 | 0.4% | 3.5% |
| Device damaged prior to usethe device was damaged before use | 1 | 0.4% | 0.3% |
| Device emits odor | 1 | 0.4% | 0.2% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Burn(s)a burn | 51 | 20.8% |
| Skin irritationirritated skin | 37 | 15.1% |
| Skin tears | 15 | 6.1% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 7 | 2.9% |
| Hypersensitivity/allergic reaction | 7 | 2.9% |
| Rashskin rash | 7 | 2.9% |
| Localized skin lesion | 5 | 2% |
| Blistera blister | 4 | 1.6% |
| Full thickness (third degree) burn | 4 | 1.6% |
| Injurya physical injury | 4 | 1.6% |
| Partial thickness (second degree) burn | 4 | 1.6% |
| Skin inflammation | 4 | 1.6% |
| Skin inflammation/ irritation | 3 | 1.2% |
| Superficial (first degree) burn | 3 | 1.2% |
| Bruise/contusion | 2 | 0.8% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Skintact | Product code GEI | All MAUDE reports |
|---|---|---|---|
| Reports | 245 | 118,290 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 4 | 4 | 9 |
| Classified as injury | 75.1% | 16.7% | 36.2% |
| Classified as malfunction | 24.5% | 80.1% | 62.3% |
| Filed by the manufacturer | 100% | 92.4% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code GEI
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| LigaSure | 8,264 | 879 | 0.2% |
| VasoView Hemopro 2 | 6,633 | 686 | 0% |
| THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S | 4,590 | 403 | 0% |
| HF unit "ESG-400" | 2,698 | 664 | 0.1% |
| Valleylab | 2,010 | 353 | 0.3% |
| Vaso View Hemopro | 1,838 | 0 | 0.1% |
| LigaSure Impact | 1,831 | 72 | 0.3% |
| THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip | 1,505 | 38 | 0.3% |
| Thunderbeat 5mm 35cm Front-Actuated Grip | 1,247 | 0 | 0.2% |
| Valleylab Ft10 | 1,203 | 2 | 0.3% |
| Vasoview Hemopro | 1,187 | 0 | 0% |
| Ligasure Advance Pistol Grip | 970 | 0 | 0% |
| Ligasure Atlas Handswitching 37cm | 924 | 0 | 0.2% |
| Edge | 859 | 171 | 0.1% |
| Force Fx | 780 | 22 | 0.4% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Skintact reports
How many FDA reports name Skintact?
245 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 17 in the latest 12 months.
What kinds of events are reported?
injury (75.1%), malfunction (24.5%) and death (0.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
insufficient device problem information (52.2%), fitting problem (3.3%), defective device (2%), device handling problem (2%) and electrical /electronic property problem (1.6%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Skintact was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.