510(k) · Cleared
ClearedVoyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Applied Medical Resources Corporation · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Oct 14, 2022 as substantially equivalent to K200598 (Applied Medical Resources Corp., 2020) after a 74-day review. Its family tree reaches back 9 generations to 1994.
- Decided
- Oct 14, 2022
- Review
- 74 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 9 generations to K932293 (1994). 17 ancestors in all. No later device cites it as a predicate yet.
- Root · 9 generations backK932293 Cabot Medical Bipolar Cutting ForcepsCabot Medical Corp. · 1994 · Recalled
- 5 generations between
- 3 generations backK182653 Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2018
- 2 generations backK193292 Voyant 5mm Fusion Device, Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2019
- 1 generation backK200598 Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2020
- This deviceK222284 Voyant Maryland Fusion device with Single-Step Activation (EB212…Applied Medical Resources Corporation · 2022
Show all 9 generations
- Root · 9 generations backK932293 Cabot Medical Bipolar Cutting ForcepsCabot Medical Corp. · 1994 · Recalled
- 8 generations backK981916 Ligasure Vessel Sealing SystemValleylab, Inc. · 1998
- 7 generations backK051644 Valleylab Forcetriad Electrosurgical GeneratorValleylab · 2005
- 6 generations backK070162 Forcetriad Electrosurgical Generator; Ligasure InstrumentsValleylab,A Division of Tyco Healthcare Group LP · 2007
- 5 generations backK141288 Voyant Electrosurgical Generator, Voyant 5MM Laparoscopic…Applied Medical Resources · 2014
- 4 generations backK172624 Voyant 5mm Fusion DeviceApplied Medical Resources Corporation · 2018
- 3 generations backK182653 Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2018
- 2 generations backK193292 Voyant 5mm Fusion Device, Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2019
- 1 generation backK200598 Voyant Maryland Fusion DeviceApplied Medical Resources Corp. · 2020
- This deviceK222284 Voyant Maryland Fusion device with Single-Step Activation (EB212…Applied Medical Resources Corporation · 2022
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K932293 | Cabot Medical Bipolar Cutting Forceps | Cabot Medical Corp. | 1994 | 3 |
| −8 | K981916 | Ligasure Vessel Sealing System | Valleylab, Inc. | 1998 | — |
| −7 | K051644 | Valleylab Forcetriad Electrosurgical Generator | Valleylab | 2005 | — |
| −6 | K070162 | Forcetriad Electrosurgical Generator; Ligasure Instruments | Valleylab,A Division of Tyco Healthcare Group LP | 2007 | — |
| −5 | K141288 | Voyant Electrosurgical Generator, Voyant 5MM Laparoscopic Sealer-Divider Device | Applied Medical Resources | 2014 | — |
| −4 | K172624 | Voyant 5mm Fusion Device | Applied Medical Resources Corporation | 2018 | — |
| −3 | K182653 | Voyant Maryland Fusion Device | Applied Medical Resources Corp. | 2018 | — |
| −2 | K193292 | Voyant 5mm Fusion Device, Voyant Maryland Fusion Device | Applied Medical Resources Corp. | 2019 | — |
| −1 | K200598 | Voyant Maryland Fusion Device | Applied Medical Resources Corp. | 2020 | — |
| 0 (this device) | K222284 | Voyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214) | Applied Medical Resources Corporation | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 4 | 0 |
| 1996 | 1 | 0 |
| 2001 | 1 | 0 |
| 2003 | 1 | 0 |
| 2009 | 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 |
|---|---|---|---|
| * | K200598 | Voyant Maryland Fusion DeviceSummary page 4…21 CFR 878.4400 Device Class: Class II Product Code: GEI Legally Marketed Voyant® Maryland Fusion Device Device: 510(k)#: K200598 Produce Code: GEI Reference Device: LigaSure Maryland Jaw Thoracic Sealer/Divider One-step Sealing… | 2020 |
| † | K181085 | LigaSure Maryland Jaw Thoracic Sealer/Divider One-step Sealing, Nano-coated | 2018 |
What descends from it?
No later submission names this one as a predicate yet.
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 28 years and passes through 7 companies; a new generation was cleared every 2.5 years on median.
- 4 of the 17 ancestors have a recall of any class.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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 Voyant Maryland Fusion Device with Single-Step Activation is a bipolar, electrosurgical device indicated for use with the Voyant electrosurgical generator in open and laparoscopic procedures where the ligation and division of vessels and tissue bundles is desired. The device can seal and divide vessels up to and including 7mm in diameter and tissue bundles that can be captured in the jaws of the device.
The device has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures, and should not be used for these procedures.
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/K222284 · printed Nov 4, 2026
Cite this page
510(k) Report. “K222284: Voyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222284
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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