510(k) Report

510(k) · Cleared

Cleared

iCE-SG2 Subcutaneous Electrode Kit

K222706510(k) TraditionalCleared Dec 6, 202290-day reviewClass II21 CFR 882.1330

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

Ice Neurosystems, Inc. · GZL Electrode, Depth

Cleared on Dec 6, 2022 as substantially equivalent to K201678 (Ice Neurosystems, Inc., 2021) after a 90-day review. Its family tree reaches back 8 generations to 1981.

Decided
Dec 6, 2022
Review
90 days
Class
Class II
Product code
GZL
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K811452 (1981). 20 ancestors in all, the oldest K802151 (1980). No later device cites it as a predicate yet.

  1. Root · 8 generations backK811452 Brown-Roberts-Wells Stereotaxic SytemTrent Wells, Inc. · 1981
  2. 7 generations backK961858 Cosgrove Depth Electrode Kit (Cdek)Radionics, Inc. · 1996
  3. 6 generations backK991522 Microtargeting ElectrodeFHC, Inc. · 2000 · Recalled
  4. 5 generations backK033173 Micro Targeting ElectrodeFHC, Inc. · 2004
  5. 4 generations backK041604 Macro-Micro Depth ElectrodeAd-Tech Medical Instrument Corp · 2004
  6. 3 generations backK053358 Depth Electrode, Foramen Ovale Depth Electrodes, Wyler Sphenoidal…Ad-Tech Medical Instrument Corp · 2006
  7. 2 generations backK163355 Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth…Ad-Tech Medical Instrument Corporation · 2017 · Recalled
  8. 1 generation backK201678 iCE-SG Subcutaneous Electrode ArraysIce Neurosystems, Inc. · 2021
  9. This deviceK222706 iCE-SG2 Subcutaneous Electrode KitIce Neurosystems, Inc. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K811452Brown-Roberts-Wells Stereotaxic SytemTrent Wells, Inc.1981—
−7K961858Cosgrove Depth Electrode Kit (Cdek)Radionics, Inc.1996—
−6K991522Microtargeting ElectrodeFHC, Inc.20003
−5K033173Micro Targeting ElectrodeFHC, Inc.2004—
−4K041604Macro-Micro Depth ElectrodeAd-Tech Medical Instrument Corp2004—
−3K053358Depth Electrode, Foramen Ovale Depth Electrodes, Wyler Sphenoidal Depth…Ad-Tech Medical Instrument Corp2006—
−2K163355Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth Electrodes…Ad-Tech Medical Instrument Corporation20175
−1K201678iCE-SG Subcutaneous Electrode ArraysIce Neurosystems, Inc.2021—
0 (this device)K222706iCE-SG2 Subcutaneous Electrode KitIce Neurosystems, Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198610
198910
199310
199510
199720
199810
199920
200510
201610
FIG. 1 — Lineage of K222706, 1981–2022Source: 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 GZL? 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 GZL device

  1. #1 K253970 Wovyn Depth Electrodescore 13.3 · 8 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
*K201678iCE-SG Subcutaneous Electrode Arrays
Summary page 4
…cate device: 510(k) Number Predicate Device Name / Manufacturer Primary Predicate iCE-SG Subcutaneous Electrode Arrays / K201678  iCE Neurosystems, Inc. DEVICE DESCR…
Ice Neurosystems, Inc.2021—

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 41 years and passes through 6 companies; a new generation was cleared every 3.9 years on median.
  • 4 of the 20 ancestors have a recall of any class.

How does its category compare?

All GZL devices

GZL Electrode, Depth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · GZL

2in 2025

2007: 32009: 12011: 12012: 12013: 12014: 12016: 22017: 42018: 32020: 12021: 32022: 32023: 32025: 22026 (partial year): 1
2007high 4 (2017) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GZL

206in 2023

2007: 166 days median2017: 222 days median2018: 58 days median2021: 262 days median2022: 90 days median2023: 206 days median
2007high 262 (2021) · low 58 (2018)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GZL

3in 2024

2008: 32009: 22014: 12021: 92024: 3
2007high 9 (2021) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GZL

12in 2025

2008: 82009: 52010: 62011: 42012: 82013: 252014: 72015: 142016: 92017: 32018: 22019: 132020: 242021: 132022: 102023: 302024: 162025: 12
2007high 30 (2023) · low 0 (2007)2025

MAUDE reports naming product code GZL, 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
2007316600
20080—38
20091—25
20100—06
20111—04
20121—08
20131—025
20141—17
20150—014
20162—09
2017422203
201835802
20190—013
20201—024
20213262913
2022390010
20233206030
20240—316
20252—012
20261—0—

What is it indicated for?

iCE-SG2 Subcutaneous Electrode Kit is intended for temporary (<14 days) use with recording and monitoring equipment for the recording and monitoring of electrical signals at the subsurface level of the brain.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222706: iCE-SG2 Subcutaneous Electrode Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K222706

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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