510(k) Report

510(k) · Cleared

Cleared

ApneaRX Pro

K223901510(k) SpecialCleared Sep 1, 2023247-day reviewClass II21 CFR 872.5570

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

Apnea Sciences Coporation · LRK Device, Anti-Snoring

Cleared on Sep 1, 2023 as substantially equivalent to K113569 (Apnea Science Corporation, 2012) after a 247-day review. Its family tree reaches back 5 generations to 2007. 1 later device descends from it.

Decided
Sep 1, 2023
Review
247 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K071404 (2007). 13 ancestors in all, the oldest K882303 (1989). 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 2 generations back: 4 other ancestors3 generations back: 2 other ancestors4 generations back: 1 other ancestor5 generations back: 1 other ancestor 1 generation forward: 1 descendant K113569 · Apnearx · Apnea Science Corporation · 2012K112205 · Snorerx 9.0 · Consumer Health Products, Inc. · 2011K103004 · Snore Guard · Ranir, LLC · 2011K100545 · Sleepright · Power Products, Inc.-Splintek · 2010K071404 · Sleep Right - Select, Low Profile and Advance · Power Products, Inc.-Splintek · 2007−50
  1. Root · 5 generations backK071404 Sleep Right - Select, Low Profile and AdvancePower Products, Inc.-Splintek · 2007
  2. 4 generations backK100545 SleeprightPower Products, Inc.-Splintek · 2010
  3. 3 generations backK103004 Snore GuardRanir, LLC · 2011
  4. 2 generations backK112205 Snorerx 9.0Consumer Health Products, Inc. · 2011
  5. 1 generation backK113569 ApnearxApnea Science Corporation · 2012
  6. This deviceK223901 ApneaRX ProApnea Sciences Coporation · 2023
  7. Descendant · cites it directly · 0 of its ownK250122 SleepRight Snore AidSplintek, Inc. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K250122SleepRight Snore AidSplintek, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K071404Sleep Right - Select, Low Profile and AdvancePower Products, Inc.-Splintek2007—
−4K100545SleeprightPower Products, Inc.-Splintek2010—
−3K103004Snore GuardRanir, LLC2011—
−2K112205Snorerx 9.0Consumer Health Products, Inc.2011—
−1K113569ApnearxApnea Science Corporation2012—
0 (this device)K223901ApneaRX ProApnea Sciences Coporation2023—
+1K250122SleepRight Snore AidSplintek, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199520
199620
199810
200410
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K223901, 2007–2025Source: 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 LRK? 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 LRK device

  1. #1 K252531 Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for…score 16.3 · 9 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
*K113569Apnearx
Summary page 4
…Product Code: LRK Regulation No. 21 CFR 872.5570 Predicate Device: ApneaRx (Apnea Sciences Corporation) (Primary predicate) Predicate 510(k) #: K113569 Reference Device 1 K203000 (KeyPrint KeySplint Hard; Keystone Industries) Reference Device 2 K170825 (SnoreRx; Apnea Scie…
Apnea Science Corporation2012—
†K203000KeyPrint KeySplint HardMycone Dental Supply Co. Inc. (Dba Keystone Industries)20211
†K170825SnoreRxApnea Sciences Corporation2017—

Also cleared against K113569: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K250122SleepRight Snore AidSplintek, Inc.20250

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 16 years and passes through 5 companies; a new generation was cleared every 9 months on median.
  • None of the 13 ancestors has a recall.
  • Of its descendants, K250122 (Splintek, Inc., 2025) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K113569.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · LRK

14in 2025

2007: 12008: 32009: 32010: 82011: 102012: 102013: 92014: 112015: 62016: 102017: 72018: 102019: 132020: 52021: 102022: 112023: 52024: 62025: 142026 (partial year): 10
2007high 14 (2025) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LRK

107in 2025

2008: 109 days median2009: 88 days median2010: 195 days median2011: 134 days median2012: 142 days median2013: 233 days median2014: 219 days median2015: 117 days median2016: 157 days median2017: 170 days median2018: 200 days median2019: 150 days median2020: 80 days median2021: 126 days median2022: 154 days median2023: 156 days median2024: 254 days median2025: 107 days median2026 (partial year): 63 days median
2007high 254 (2024) · low 80 (2020)2026

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

Recalls per year · LRK

1in 2025

2009: 22025: 12026 (partial year): 1
2007high 2 (2009) · low 0 (2007)2026

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

Adverse event reports per year · LRK

653in 2025

2008: 12009: 112010: 72011: 692012: 4452013: 722014: 492015: 282016: 182017: 322018: 612019: 562020: 242021: 492022: 402023: 502024: 1852025: 653
2007high 653 (2025) · low 0 (2007)2025

MAUDE reports naming product code LRK, 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
20071—00
2008310901
2009388211
2010819507
201110134069
2012101420445
20139233072
201411219049
20156117028
201610157018
20177170032
201810200061
201913150056
2020580024
202110126049
202211154040
20235156050
202462540185
2025141071653
202610631—

What is it indicated for?

The ApneaRx Pro is intended for use on adult patients 18 years of age or older as an aid for the reduction of mild to moderate obstructive sleep apnea (OSA), and/or snoring.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223901: ApneaRX Pro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K223901

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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