510(k) Report

510(k) · Cleared

Cleared

Tap Iii Anti-Snoring Device

K062951510(k) TraditionalCleared Dec 12, 200674-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

Airway Management, Inc. · LRK Device, Anti-Snoring

Cleared on Dec 12, 2006 as substantially equivalent to K962516 (Nellcor Puritan Bennett, Inc., 1996) and 2 other predicates after a 74-day review. Its family tree reaches back 6 generations to 1989. 15 later devices descend from it.

Decided
Dec 12, 2006
Review
74 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K882303 (1989). 10 ancestors in all. 15 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor1993: 1 other ancestor1999: 1 other ancestor1997: 1 other ancestor2009: 1 descendant cleared2011: 2 descendants cleared2016: 2 descendants cleared2021: 2 descendants cleared2012: 1 descendant cleared2019: 2 descendants cleared2017: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant cleared2026: 1 descendant cleared2025: 1 descendant clearedK882303 · H&M Anti-Snoring Device · Hays & Meade, Inc. · 1989K962516 · Tap Anti-Snoring Device · Nellcor Puritan Bennett, Inc. · 1996K972061 · TOA · W. Keith Thornton, D.D.S. · 1997K022891 · The Breathe EZ Anti-Snoring Device · D&S Redhage · 2003K030440 · Oasys-Oral Airway System · Mark Abramson, D.D.S., Inc. · 2003K060388 · Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with Attachment · Airway Management, Inc. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors3 generations back: 2 other ancestors 1 generation forward: 6 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant4 generations forward: 2 descendants5 generations forward: 2 descendants6 generations forward: 1 descendant K060388 · Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with Attachment · Airway Management, Inc. · 2006K030440 · Oasys-Oral Airway System · Mark Abramson, D.D.S., Inc. · 2003K022891 · The Breathe EZ Anti-Snoring Device · D&S Redhage · 2003K972061 · TOA · W. Keith Thornton, D.D.S. · 1997K962516 · Tap Anti-Snoring Device · Nellcor Puritan Bennett, Inc. · 1996K882303 · H&M Anti-Snoring Device · Hays & Meade, Inc. · 1989−50+5
  1. Root · 6 generations backK882303 H&M Anti-Snoring DeviceHays & Meade, Inc. · 1989
  2. 5 generations backK962516 Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc. · 1996
  3. 4 generations backK972061 TOAW. Keith Thornton, D.D.S. · 1997
  4. 3 generations backK022891 The Breathe EZ Anti-Snoring DeviceD&S Redhage · 2003
  5. 2 generations backK030440 Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc. · 2003
  6. 1 generation backK060388 Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with…Airway Management, Inc. · 2006
  7. This deviceK062951 Tap Iii Anti-Snoring DeviceAirway Management, Inc. · 2006
  8. Descendant · cites it directly · 8 of its ownK160234 OVENTOventus Manufacturing Pty, Ltd. · 2016
  9. Descendant · cites it directly · 7 of its ownK161832 O2VENT TOventus Manufacturing Pty, Ltd. · 2016
  10. Descendant · 2 generations on · 6 of its ownK171316 O2Vent WOventus Manufacturing Pty, Ltd. · 2017
  11. Descendant · 3 generations on · 5 of its ownK190236 O2Vent OptimaOventus Manufacturing Pty, Ltd. · 2019
  12. Descendant · 4 generations on · 3 of its ownK203606 Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep…Meris Investment Group · 2021

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2009: 12011: 22012: 12016: 22017: 12019: 22021: 22022: 12024: 12025: 12026: 1
2009high 2 (2011) · low 0 (2010)2026

Most influential descendants

Showing 5 of 15 · See all
  • K160234OVENTOventus Manufacturing Pty, Ltd. · 2016 · cites it directly8descendants
  • K161832O2VENT TOventus Manufacturing Pty, Ltd. · 2016 · cites it directly7descendants
  • K171316O2Vent WOventus Manufacturing Pty, Ltd. · 2017 · 2 generations on6descendants
  • K190236O2Vent OptimaOventus Manufacturing Pty, Ltd. · 2019 · 3 generations on5descendants
  • K203606Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic Mandibular…Meris Investment Group · 2021 · 4 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K882303H&M Anti-Snoring DeviceHays & Meade, Inc.1989—
−5K962516Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc.1996—
−4K972061TOAW. Keith Thornton, D.D.S.1997—
−3K022891The Breathe EZ Anti-Snoring DeviceD&S Redhage2003—
−2K030440Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc.2003—
−1K060388Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with AttachmentAirway Management, Inc.2006—
0 (this device)K062951Tap Iii Anti-Snoring DeviceAirway Management, Inc.2006—
+1K160234OVENTOventus Manufacturing Pty, Ltd.2016—
+1K161832O2VENT TOventus Manufacturing Pty, Ltd.2016—
+2K171316O2Vent WOventus Manufacturing Pty, Ltd.2017—
+3K190236O2Vent OptimaOventus Manufacturing Pty, Ltd.2019—
+4K203606Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic…Meris Investment Group2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199610
199710
199910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201120
201210
201620
201710
201920
202120
202210
202410
202510
202610
FIG. 1 — Lineage of K062951, 1989–2026Source: 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? (3)

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
*K962516Tap Anti-Snoring Device
Summary page 1
…me Anti -Snoring / Obstructive Sleep Apnea Device Device: TAP III Predicate Device Nellcor Puritan Bennett - TAP-K9625 16 Thornton Oral Appliance - TOA-K972061 TAP 11 K060388 DV t&1V…
Nellcor Puritan Bennett, Inc.1996—
*K972061TOA
Summary page 1
…TAP III Predicate Device Nellcor Puritan Bennett - TAP-K9625 16 Thornton Oral Appliance - TOA-K972061 TAP 11 K060388 DV t&1Vsi tioa: -< -- M The TAP III Anti-Snori…
W. Keith Thornton, D.D.S.1997—
*K060388Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with Attachment
Summary page 1
…Nellcor Puritan Bennett - TAP-K9625 16 Thornton Oral Appliance - TOA-K972061 TAP 11 K060388 DV t&1Vsi tioa: -< -- M The TAP III Anti-Snoring device is comprised of: *Lower t…
Airway Management, Inc.2006—

Also cleared against K962516: 12 other devices →

What descends from it? (15)

See all 15

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

NumberDeviceApplicantDecidedDescendants
K160234OVENTOventus Manufacturing Pty, Ltd.20168
K161832O2VENT TOventus Manufacturing Pty, Ltd.20167
K111110Apnea GuardAdvanced Brain Monitoring, Inc.20112
K203477ClassicOrthoapnea S.L.20210
K102521Pantino Pro PositinerSomnomed, Inc.20110
K090911Ist Snoring ApplianceDental Crafters20090

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 17 years and passes through 6 companies; a new generation was cleared every 2.7 years on median.
  • None of the 10 ancestors has a recall.
  • Of its descendants, K160234 (Oventus Manufacturing Pty, Ltd., 2016) has gone furthest, with 8 descendants of its own.
  • 12 other devices also cite its predicate K962516.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years.

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?

To reduce or alleviate night time snoring and mild to moderate obstructive sleep apnea (OSA).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K062951: Tap Iii Anti-Snoring Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062951

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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