510(k) · Cleared
ClearedVapr Arctic Suction Electrode
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Depuy Mitek, A Johnson & Johnson Company · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Aug 5, 2014 as substantially equivalent to K113545 (Depuy Mitek, A Johnson & Johnson Company, 2012) and 4 other predicates after a 119-day review. Its family tree reaches back 11 generations to 1993.
- Decided
- Aug 5, 2014
- Review
- 119 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 5
Its longest line of descent runs back 11 generations to K931783 (1993). 68 ancestors in all, the oldest K852143 (1985). No later device cites it as a predicate yet.
- Root · 11 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
- 7 generations between
- 3 generations backK053510 IR Wireless Foot SwitchLinemaster Switch Corp. · 2006 · Recalled
- 2 generations backK083161 Zen Wireless Footswitch (W1000), Zen Wireless Footswitch Adapter…Conmed Linvatec · 2009
- 1 generation backK100638 Vapr Vue Radiofrequency System ,Model 225024, VPR Vue Wireless…Depuy Mitek, A Johnson & Johnson Company · 2010
- This deviceK140896 Vapr Arctic Suction ElectrodeDepuy Mitek, A Johnson & Johnson Company · 2014
Show all 11 generations
- Root · 11 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
- 10 generations backK960655 Aesop System and AccessoriesComputer Motion, Inc. · 1996
- 9 generations backK973700 Hermes Operating Room Control CenterComputer Motion, Inc. · 1998
- 8 generations backK980787 Hermes Operating Room Control Center with the Wom 20L InsufflatorComputer Motion, Inc. · 1998
- 7 generations backK990691 Hermes Operating Room Control CenterComputer Motion, Inc. · 1999
- 6 generations backK991444 Hermes Control Center, with Control of the Aesop 3000HR (Hermes…Computer Motion, Inc. · 1999
- 5 generations backK022393 Merdoc SystemStryker Endoscopy · 2003
- 4 generations backK033135 Stryker Wireless Universal Footswitch SystemStryker Endoscopy · 2004
- 3 generations backK053510 IR Wireless Foot SwitchLinemaster Switch Corp. · 2006 · Recalled
- 2 generations backK083161 Zen Wireless Footswitch (W1000), Zen Wireless Footswitch Adapter…Conmed Linvatec · 2009
- 1 generation backK100638 Vapr Vue Radiofrequency System ,Model 225024, VPR Vue Wireless…Depuy Mitek, A Johnson & Johnson Company · 2010
- This deviceK140896 Vapr Arctic Suction ElectrodeDepuy Mitek, A Johnson & Johnson Company · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K931783 | Aesop (Automated Endoscopic System for Optimal Pos | Computer Motion, Inc. | 1993 | — |
| −10 | K960655 | Aesop System and Accessories | Computer Motion, Inc. | 1996 | — |
| −9 | K973700 | Hermes Operating Room Control Center | Computer Motion, Inc. | 1998 | — |
| −8 | K980787 | Hermes Operating Room Control Center with the Wom 20L Insufflator | Computer Motion, Inc. | 1998 | — |
| −7 | K990691 | Hermes Operating Room Control Center | Computer Motion, Inc. | 1999 | — |
| −6 | K991444 | Hermes Control Center, with Control of the Aesop 3000HR (Hermes Ready). | Computer Motion, Inc. | 1999 | — |
| −5 | K022393 | Merdoc System | Stryker Endoscopy | 2003 | — |
| −4 | K033135 | Stryker Wireless Universal Footswitch System | Stryker Endoscopy | 2004 | — |
| −3 | K053510 | IR Wireless Foot Switch | Linemaster Switch Corp. | 2006 | 2 |
| −2 | K083161 | Zen Wireless Footswitch (W1000), Zen Wireless Footswitch Adapter (W1100) | Conmed Linvatec | 2009 | — |
| −1 | K100638 | Vapr Vue Radiofrequency System ,Model 225024, VPR Vue Wireless Footswitch… | Depuy Mitek, A Johnson & Johnson Company | 2010 | — |
| 0 (this device) | K140896 | Vapr Arctic Suction Electrode | Depuy Mitek, A Johnson & Johnson Company | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1985 | 1 | 0 |
| 1986 | 2 | 0 |
| 1989 | 1 | 0 |
| 1991 | 1 | 0 |
| 1994 | 3 | 0 |
| 1995 | 5 | 0 |
| 1996 | 3 | 0 |
| 1997 | 4 | 0 |
| 1998 | 3 | 0 |
| 1999 | 5 | 0 |
| 2000 | 10 | 0 |
| 2001 | 6 | 0 |
| 2002 | 3 | 0 |
| 2003 | 3 | 0 |
| 2004 | 2 | 0 |
| 2005 | 2 | 0 |
| 2008 | 1 | 0 |
| 2012 | 2 | 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? (6)
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 |
|---|---|---|---|
| * | K113545 | Vapr Vue Generator, Vapr 3 Electrosurgical System, Vapr II Electrosurgical System…Summary page 5…icate The proposed VAPR ARCTIC Electrode is substantially Device(s) equivalent to: CP90 Electrode: K113545/ K100638 o (November 11, 2012/ June 18, 2010) P50 Electr… | 2012 |
| * | K100638 | Vapr Vue Radiofrequency System ,Model 225024, VPR Vue Wireless Footswitch, Model 227214Summary page 5…The proposed VAPR ARCTIC Electrode is substantially Device(s) equivalent to: CP90 Electrode: K113545/ K100638 o (November 11, 2012/ June 18, 2010) P50 Electrode: K122… | 2010 |
| * | K122425 | Vapr P50 Suction Electrode Vapr S90 Suction Electrode Vapr P50 Suction Electrode with…Summary page 5… CP90 Electrode: K113545/ K100638 o (November 11, 2012/ June 18, 2010) P50 Electrode: K122425/ K100638/K082643: o (November 11, 2012/June 18, 2010) Sm… | 2012 |
| * | K082643 | 3.5 MM Side Effect Electrode with Integrated Handpiece, Model 227301, 3.5 MM Angled Side…Summary page 5…Electrode: K113545/ K100638 o (November 11, 2012/ June 18, 2010) P50 Electrode: K122425/ K100638/K082643: o (November 11, 2012/June 18, 2010) Smith and Nephew Ef… | 2008 |
| * | K000691 | Vulcan Electrosurgical Probes: Vulcan Micro Ligament Chisels, Vulcan Ligament Chisels…Summary page 5…de: K122425/ K100638/K082643: o (November 11, 2012/June 18, 2010) Smith and Nephew Eflex Ablator K000691 o (May 4, 2000) Arthrocare Hip ArthroWand: 510(k) # Not… | 2000 |
| * | — | Arthrocare Hip ArthroWand Named without a submission number |
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 21 years and passes through 5 companies; a new generation was cleared every 1.6 years on median.
- 11 of the 68 ancestors have a recall of any class.
- 3 other devices also cite its predicate K113545.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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 VAPR® ARCTIC™ Suction Electrode for use with the VAPR VUE® RF System is intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissue in patients requiring arthroscopic surgery of the hip.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140896 · printed Nov 5, 2026
Cite this page
510(k) Report. “K140896: Vapr Arctic Suction Electrode.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K140896
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