510(k) · Cleared
ClearedgammaCore-2
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Eletrocore, LLC · PKR Non-Invasive Vagus Nerve Stimulator - Headache
Cleared on Dec 7, 2017 as substantially equivalent to K171306 (Electrocore, LLC, 2017) after a 132-day review. Its family tree reaches back 2 generations to 2017. 5 later devices descend from it.
- Decided
- Dec 7, 2017
- Review
- 132 days
- Class
- Class II
- Product code
- PKR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to DEN150048 (2017). 5 later devices descend from it, 1 citing it directly.
- Root · 2 generations backDEN150048 gammaCore Non-invasive Vagus Nerve StimulatorElectrocore, LLC · 2017
- 1 generation backK171306 gammaCore-SElectrocore, LLC · 2017
- This deviceK172270 gammaCore-2Eletrocore, LLC · 2017
- Descendant · cites it directly · 4 of its ownK180538 gammaCore SapphireElectrocore, LLC · 2018
- Descendant · 2 generations on · 3 of its ownK182369 gammaCore SapphireElectrocore, Inc. · 2018
- Descendant · 3 generations on · 2 of its ownK191830 gammaCore SapphireElectrocore, Inc. · 2020
- Descendant · 4 generations on · 1 of its ownK203546 gammaCore SapphireElectrocore, Inc. · 2021
- Descendant · 5 generations on · 0 of its ownK211856 gammaCore SapphireElectrocore, Inc. · 2021
Most influential descendants
Showing 5 of 5 · See all- K180538gammaCore SapphireElectrocore, LLC · 2018 · cites it directly4descendants
- K182369gammaCore SapphireElectrocore, Inc. · 2018 · 2 generations on3descendants
- K191830gammaCore SapphireElectrocore, Inc. · 2020 · 3 generations on2descendants
- K203546gammaCore SapphireElectrocore, Inc. · 2021 · 4 generations on1descendant
- K211856gammaCore SapphireElectrocore, Inc. · 2021 · 5 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | DEN150048 | gammaCore Non-invasive Vagus Nerve Stimulator | Electrocore, LLC | 2017 | — |
| −1 | K171306 | gammaCore-S | Electrocore, LLC | 2017 | — |
| 0 (this device) | K172270 | gammaCore-2 | Eletrocore, LLC | 2017 | — |
| +1 | K180538 | gammaCore Sapphire | Electrocore, LLC | 2018 | — |
| +2 | K182369 | gammaCore Sapphire | Electrocore, Inc. | 2018 | — |
| +3 | K191830 | gammaCore Sapphire | Electrocore, Inc. | 2020 | — |
| +4 | K203546 | gammaCore Sapphire | Electrocore, Inc. | 2021 | — |
| +5 | K211856 | gammaCore Sapphire | Electrocore, Inc. | 2021 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 2 | 0 |
| 2020 | 1 | 0 |
| 2021 | 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 PKR? 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 PKR device
- #1 K203546 gammaCore Sapphirescore 5.3 · 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? (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 |
|---|---|---|---|
| * | K171306 | gammaCore-SSummary page 5…t Codes: PKR Page 1 of 4 K172270 Predicate Device: gammaCore-S K171306 Device Description: gammaCore-2 is a device that provides non-invasive Vagus Nerve Stimulation (nVNS) when applied to the side o… | 2017 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K180538 | gammaCore Sapphire | 2018 | 4 |
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 0 years and passes through 2 companies; a new generation was cleared every 6 months on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K180538 (Electrocore, LLC, 2018) has gone furthest, with 4 descendants of its own.
- 1 other device also cites its predicate K171306.
How does its category compare?
All PKR devicesPKR Non-Invasive Vagus Nerve Stimulator - Headache: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · PKR
2in 2021
2026 to Oct 25, outlined.
Median 510(k) review, days · PKR
78in 2018
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PKR
No recall names PKR since 2007.
Adverse event reports per year · PKR
1in 2018
MAUDE reports naming product code PKR, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 3 | — | 0 | 0 |
| 2018 | 3 | 78 | 0 | 1 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 2 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The gammaCore-2 Non-invasive Vagus Nerve Stimulator is intended to
provide noninvasive vagus nerve stimulation (nVNS) on the side of the neck. The gammaCore -2
device is indicated for the acute treatment of pain associated with episodic cluster headache in
adult patients.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K172270 · printed Nov 6, 2026
Cite this page
510(k) Report. “K172270: gammaCore-2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172270
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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