510(k) Report

510(k) · Cleared

Cleared

Progenix Select Stim

K242460510(k) TraditionalCleared Apr 2, 2025226-day reviewClass II21 CFR 882.5890

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

Progenix, LLC · NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

Cleared on Apr 2, 2025 as substantially equivalent to K190347 (Hivox Biotek, Inc., 2019) and 1 other predicate after a 226-day review. Its family tree reaches back 8 generations to 1994.

Decided
Apr 2, 2025
Review
226 days
Class
Class II
Product code
NUH
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K940301 (1994). 11 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK940301 Compex 2Biodex Medical Systems, Inc. · 1994
  2. 7 generations backK011880 Compex SportCompex S.A. · 2002
  3. 6 generations backK060846 Therapeutic Massage CompanionEndurance Therapeutics · 2007
  4. 5 generations backK110068 Model PM3030Omron Healthcare, Inc. · 2011
  5. 4 generations backK132993 Counter Otc Tens DeviceCounter Scientific Development (Gz), Ltd. · 2014
  6. 3 generations backK150386 Tyece OTC TENS DeviceTyece, Ltd. · 2015
  7. 2 generations backK171803 HIVOX OTC Electrical StimulatorHivox Biotek, Inc. · 2017
  8. 1 generation backK190347 HIVOX OTC Electrical StimulatorHivox Biotek, Inc. · 2019
  9. This deviceK242460 Progenix Select StimProgenix, LLC · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K940301Compex 2Biodex Medical Systems, Inc.1994—
−7K011880Compex SportCompex S.A.2002—
−6K060846Therapeutic Massage CompanionEndurance Therapeutics2007—
−5K110068Model PM3030Omron Healthcare, Inc.2011—
−4K132993Counter Otc Tens DeviceCounter Scientific Development (Gz), Ltd.2014—
−3K150386Tyece OTC TENS DeviceTyece, Ltd.2015—
−2K171803HIVOX OTC Electrical StimulatorHivox Biotek, Inc.2017—
−1K190347HIVOX OTC Electrical StimulatorHivox Biotek, Inc.2019—
0 (this device)K242460Progenix Select StimProgenix, LLC2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
201310
FIG. 1 — Lineage of K242460, 1994–2025Source: 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 NUH? 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 NUH device

  1. #1 K190783 Health Expert Electronic Stimulator (model…score 15.8 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K190347HIVOX OTC Electrical Stimulator
Summary page 5
…HIVOX OTC Electrical Stimulator Model Number EM49-1, EM49-2 510(k) Number K190347, K171803 Product Code NUH, NGX Panel Code Neurology Regulation Number…
Hivox Biotek, Inc.2019—
*K171803HIVOX OTC Electrical Stimulator
Summary page 5
…HIVOX OTC Electrical Stimulator Model Number EM49-1, EM49-2 510(k) Number K190347, K171803 Product Code NUH, NGX Panel Code Neurology Regulation Number 21…
Hivox Biotek, Inc.2017—
†K160138Adhesive ElectrodesGmdasz Manufacturing Co., Ltd.2016—

Also cleared against K190347: 2 other devices →

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 31 years and passes through 8 companies; a new generation was cleared every 4.0 years on median.
  • None of the 11 ancestors has a recall.
  • 2 other devices also cite its predicate K190347.

How does its category compare?

All NUH devices

NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · NUH

15in 2025

2007: 42009: 12010: 32011: 62012: 62013: 102014: 162015: 142016: 132017: 172018: 162019: 192020: 142021: 142022: 202023: 152024: 202025: 152026 (partial year): 5
2007high 20 (2022) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NUH

119in 2025

2007: 161 days median2010: 148 days median2011: 231 days median2012: 170 days median2013: 189 days median2014: 212 days median2015: 198 days median2016: 145 days median2017: 155 days median2018: 121 days median2019: 213 days median2020: 147 days median2021: 198 days median2022: 103 days median2023: 127 days median2024: 90 days median2025: 119 days median2026 (partial year): 137 days median
2007high 231 (2011) · low 90 (2024)2026

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

Recalls per year · NUH

No recall names NUH since 2007.

Adverse event reports per year · NUH

7in 2025

2013: 12014: 92015: 112016: 132017: 212018: 182019: 52020: 82021: 72022: 22023: 42024: 72025: 7
2007high 21 (2017) · low 0 (2007)2025

MAUDE reports naming product code NUH, 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
2007416100
20080—00
20091—00
2010314800
2011623100
2012617000
20131018901
20141621209
201514198011
201613145013
201717155021
201816121018
20191921305
20201414708
20211419807
20222010302
20231512704
2024209007
20251511907
202651370—

What is it indicated for?

TENS:

Temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities (arm), lower extremities (leg), abdomen and bottom due to strain from exercise or normal household work activities.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K242460: Progenix Select Stim.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K242460

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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