510(k) Report

510(k) · Cleared

Cleared

SnoreRx

K170825510(k) AbbreviatedCleared Aug 18, 2017151-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 Corporation · LRK Device, Anti-Snoring

Cleared on Aug 18, 2017 as substantially equivalent to K153200 (Apnea Sciences Corporation, 2016) after a 151-day review. Its family tree reaches back 5 generations to 2007. 21 later devices descend from it.

Decided
Aug 18, 2017
Review
151 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K071404 (2007). 10 ancestors in all, the oldest K882303 (1989). 21 later devices descend from it, 11 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1998: 1 other ancestor1995: 2 other ancestors2010: 1 other ancestor1989: 1 other ancestor2018: 2 descendants cleared2026: 6 descendants cleared2025: 6 descendants cleared2020: 1 descendant cleared2019: 1 descendant cleared2021: 3 descendants cleared2024: 2 descendants clearedK071404 · Sleep Right - Select, Low Profile and Advance · Power Products, Inc.-Splintek · 2007K100545 · Sleepright · Power Products, Inc.-Splintek · 2010K103004 · Snore Guard · Ranir, LLC · 2011K112205 · Snorerx 9.0 · Consumer Health Products, Inc. · 2011K153200 · SnoreRx · Apnea Sciences Corporation · 20161990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 3 other ancestors4 generations back: 1 other ancestor5 generations back: 1 other ancestor 1 generation forward: 11 descendants2 generations forward: 8 descendants3 generations forward: 2 descendants K153200 · SnoreRx · Apnea Sciences Corporation · 2016K112205 · 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 backK153200 SnoreRxApnea Sciences Corporation · 2016
  6. This deviceK170825 SnoreRxApnea Sciences Corporation · 2017
  7. Descendant · cites it directly · 3 of its ownK233850 Difiney Anti Snoring DeviceFissiontech, LLC · 2024
  8. Descendant · cites it directly · 3 of its ownK191618 SleepTight Mouthpiece STZMichael D Williams Dds PA · 2019
  9. Descendant · cites it directly · 2 of its ownK200657 SmartGuard Anti-Snoring DeviceSmartguard Rx, Inc. · 2021
  10. Descendant · cites it directly · 1 of its ownK253845 Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB…Ram.Shaw Pte., Ltd. · 2026
  11. Descendant · 2 generations on · 1 of its ownK252531 Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)Myofunctional Research Co. · 2026

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

2018: 22019: 12020: 12021: 32024: 22025: 62026: 6
2018high 6 (2025) · low 0 (2022)2026

Most influential descendants

Showing 5 of 21 · See all
  • K233850Difiney Anti Snoring DeviceFissiontech, LLC · 2024 · cites it directly3descendants
  • K191618SleepTight Mouthpiece STZMichael D Williams Dds PA · 2019 · cites it directly3descendants
  • K200657SmartGuard Anti-Snoring DeviceSmartguard Rx, Inc. · 2021 · cites it directly2descendants
  • K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte., Ltd. · 2026 · cites it directly1descendant
  • K252531Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)Myofunctional Research Co. · 2026 · 2 generations on1descendant
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—
−1K153200SnoreRxApnea Sciences Corporation2016—
0 (this device)K170825SnoreRxApnea Sciences Corporation2017—
+1K233850Difiney Anti Snoring DeviceFissiontech, LLC2024—
+1K191618SleepTight Mouthpiece STZMichael D Williams Dds PA2019—
+1K200657SmartGuard Anti-Snoring DeviceSmartguard Rx, Inc.2021—
+1K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte., Ltd.2026—
+2K252531Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)Myofunctional Research Co.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199520
199810
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201820
201910
202010
202130
202420
202560
202660
FIG. 1 — Lineage of K170825, 2007–2026Source: 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
*K153200SnoreRx
Summary page 4
…Class II Product Code: LRK Regulation No. 21 CFR 872.5570 Predicate Device: SnoreRx (Apnea Sciences Corporation) Predicate 510(k) #: K153200 Device Description: The SnoreRx is an intraoral device that repositions the jaw anteriorly in orde…
Apnea Sciences Corporation2016—

What descends from it? (21)

See all 21

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

NumberDeviceApplicantDecidedDescendants
K233850Difiney Anti Snoring DeviceFissiontech, LLC20243
K191618SleepTight Mouthpiece STZMichael D Williams Dds PA20193
K200657SmartGuard Anti-Snoring DeviceSmartguard Rx, Inc.20212
K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte., Ltd.20261
K201484Somnos Anti-Snoring Mouth GuardKoncept Innovators, LLC20201
K252161Hushd AveraGood Sleep CO Pte, Ltd.20250
K251628Mandibular Advancement Device L07Dcstar, Inc.20250
K250122SleepRight Snore AidSplintek, Inc.20250
K203462Advanced Dental ApplianceDasoft Partners20210
K181396Oral Device OA, Oral Device SPassion For Life Healthcare (Uk) Limited20180

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 10 years and passes through 4 companies; a new generation was cleared every 1.0 years on median.
  • None of the 10 ancestors has a recall.
  • Of its descendants, K233850 (Fissiontech, LLC, 2024) has gone furthest, with 3 descendants of its own.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, 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 SnoreRx is intended for use on adult patients 18 years of age or older as an aid for the reduction of snoring.

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. “K170825: SnoreRx.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K170825

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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