510(k) Report

510(k) · Cleared

Cleared

gammaCore-S

K171306510(k) SpecialCleared May 30, 201727-day reviewClass II21 CFR 882.5892

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Electrocore, LLC · PKR Non-Invasive Vagus Nerve Stimulator - Headache

Cleared on May 30, 2017 as substantially equivalent to DEN150048 (Electrocore, LLC, 2017) after a 27-day review. Its family tree reaches back 1 generation to 2017. 7 later devices descend from it.

Decided
May 30, 2017
Review
27 days
Class
Class II
Product code
PKR
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to DEN150048 (2017). 7 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2018: 3 descendants cleared2017: 1 descendant cleared2020: 1 descendant cleared2021: 2 descendants clearedDEN150048 · gammaCore Non-invasive Vagus Nerve Stimulator · Electrocore, LLC · 2017201620182020202220242026
Descendants, by generation 1 generation forward: 2 descendants2 generations forward: 1 descendant3 generations forward: 1 descendant4 generations forward: 1 descendant5 generations forward: 1 descendant6 generations forward: 1 descendant DEN150048 · gammaCore Non-invasive Vagus Nerve Stimulator · Electrocore, LLC · 20170+5
  1. Root · 1 generation backDEN150048 gammaCore Non-invasive Vagus Nerve StimulatorElectrocore, LLC · 2017
  2. This deviceK171306 gammaCore-SElectrocore, LLC · 2017
  3. Descendant · cites it directly · 5 of its ownK172270 gammaCore-2Eletrocore, LLC · 2017
  4. Descendant · 2 generations on · 4 of its ownK180538 gammaCore SapphireElectrocore, LLC · 2018
  5. Descendant · 3 generations on · 3 of its ownK182369 gammaCore SapphireElectrocore, Inc. · 2018
  6. Descendant · 4 generations on · 2 of its ownK191830 gammaCore SapphireElectrocore, Inc. · 2020
  7. Descendant · 5 generations on · 1 of its ownK203546 gammaCore SapphireElectrocore, Inc. · 2021

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2017: 12018: 32020: 12021: 2
2017high 3 (2018) · low 0 (2019)2026

Most influential descendants

Showing 5 of 7 · See all
  • K172270gammaCore-2Eletrocore, LLC · 2017 · cites it directly5descendants
  • K180538gammaCore SapphireElectrocore, LLC · 2018 · 2 generations on4descendants
  • K182369gammaCore SapphireElectrocore, Inc. · 2018 · 3 generations on3descendants
  • K191830gammaCore SapphireElectrocore, Inc. · 2020 · 4 generations on2descendants
  • K203546gammaCore SapphireElectrocore, Inc. · 2021 · 5 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1DEN150048gammaCore Non-invasive Vagus Nerve StimulatorElectrocore, LLC2017—
0 (this device)K171306gammaCore-SElectrocore, LLC2017—
+1K172270gammaCore-2Eletrocore, LLC2017—
+2K180538gammaCore SapphireElectrocore, LLC2018—
+3K182369gammaCore SapphireElectrocore, Inc.2018—
+4K191830gammaCore SapphireElectrocore, Inc.2020—
+5K203546gammaCore SapphireElectrocore, Inc.2021—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201830
202010
202120
FIG. 1 — Lineage of K171306, 2017–2021Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K203546 gammaCore Sapphirescore 5.3 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*DEN150048gammaCore Non-invasive Vagus Nerve Stimulator
Summary page 5
…Page 18 of 39 gammaCore-S® Special 510(k) Premarket Application Predicate Device: gammaCore-DEN150048 Device Description: gammaCore-S is a device that provides non-invasive Vagus Nerve Stimulation (nVNS) when applied to the side o…
Electrocore, LLC2017—

What descends from it? (7)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K172270gammaCore-2Eletrocore, LLC20175
K173442gammaCore-SElectrocore, LLC20180

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?

  • Its one ancestor has no recall.
  • Of its descendants, K172270 (Eletrocore, LLC, 2017) has gone furthest, with 5 descendants of its own.

How does its category compare?

All PKR devices

PKR 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

2017: 32018: 32020: 12021: 2
2007high 3 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PKR

78in 2018

2018: 78 days median
2007high 78 (2018)2026

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

2018: 1
2007high 1 (2018) · low 0 (2007)2025

MAUDE reports naming product code PKR, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20173—00
201837801
20190—00
20201—00
20212—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The gammaCore-S Non-invasive Vagus Nerve Stimulator is intended to provide noninvasive vagus nerve stimulation (nVNS) on the side of the neck. The gammaCore -S 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.

Cite this page

510(k) Report. “K171306: gammaCore-S.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171306

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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