510(k) Report

510(k) · Cleared

Cleared

Respire Pink Series - Herbst

K131138510(k) TraditionalCleared Sep 9, 2013139-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

Respire Medical · LRK Device, Anti-Snoring

Cleared on Sep 9, 2013 as substantially equivalent to K111207 (Respire Medical, 2011) and 1 other predicate after a 139-day review. Its family tree reaches back 7 generations to 1989. 7 later devices descend from it.

Decided
Sep 9, 2013
Review
139 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K882303 (1989). 16 ancestors in all. 7 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 1 other ancestor2008: 1 other ancestor2005: 1 other ancestor1996: 2 other ancestors2004: 1 other ancestor1999: 1 other ancestor1997: 1 other ancestor1993: 1 other ancestor2023: 1 descendant cleared2015: 1 descendant cleared2017: 1 descendant cleared2014: 1 descendant cleared2020: 2 descendants cleared2022: 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. · 2006K111207 · Respire Blue Series · Respire Medical · 20111990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 3 other ancestors4 generations back: 2 other ancestors 1 generation forward: 4 descendants2 generations forward: 2 descendants3 generations forward: 1 descendant K111207 · Respire Blue Series · Respire Medical · 2011K060388 · 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
  1. Root · 7 generations backK882303 H&M Anti-Snoring DeviceHays & Meade, Inc. · 1989
  2. 6 generations backK962516 Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc. · 1996
  3. 5 generations backK972061 TOAW. Keith Thornton, D.D.S. · 1997
  4. 4 generations backK022891 The Breathe EZ Anti-Snoring DeviceD&S Redhage · 2003
  5. 3 generations backK030440 Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc. · 2003
  6. 2 generations backK060388 Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with…Airway Management, Inc. · 2006
  7. 1 generation backK111207 Respire Blue SeriesRespire Medical · 2011
  8. This deviceK131138 Respire Pink Series - HerbstRespire Medical · 2013
  9. Descendant · cites it directly · 5 of its ownK150572 Respire Pink Series-Herbst-EFRespire Medical Holding · 2015 · Recalled
  10. Descendant · cites it directly · 2 of its ownK170692 Respire Pink Series with DentiTracRespire Medical Holding · 2017
  11. Descendant · 2 generations on · 1 of its ownK192127 Respire Pink AT (Hard, Hard/Soft, EF)Respire Medical Holdings · 2020
  12. Descendant · cites it directly · 0 of its ownK223624 Emerald HerbstIsland Dental Lab, Inc Dba Emerald Dental · 2023
  13. Descendant · 3 generations on · 0 of its ownK214096 Respire ClearRespire Medical, LLC · 2022

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2014: 12015: 12017: 12020: 22022: 12023: 1
2014high 2 (2020) · low 0 (2016)2026

Most influential descendants

Showing 5 of 7 · See all
  • K150572Respire Pink Series-Herbst-EFRespire Medical Holding · 2015 · cites it directly5descendants
  • K170692Respire Pink Series with DentiTracRespire Medical Holding · 2017 · cites it directly2descendants
  • K192127Respire Pink AT (Hard, Hard/Soft, EF)Respire Medical Holdings · 2020 · 2 generations on1descendant
  • K223624Emerald HerbstIsland Dental Lab, Inc Dba Emerald Dental · 2023 · cites it directly0descendants
  • K214096Respire ClearRespire Medical, LLC · 2022 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K882303H&M Anti-Snoring DeviceHays & Meade, Inc.1989—
−6K962516Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc.1996—
−5K972061TOAW. Keith Thornton, D.D.S.1997—
−4K022891The Breathe EZ Anti-Snoring DeviceD&S Redhage2003—
−3K030440Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc.2003—
−2K060388Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with AttachmentAirway Management, Inc.2006—
−1K111207Respire Blue SeriesRespire Medical2011—
0 (this device)K131138Respire Pink Series - HerbstRespire Medical2013—
+1K150572Respire Pink Series-Herbst-EFRespire Medical Holding20153
+1K170692Respire Pink Series with DentiTracRespire Medical Holding2017—
+2K192127Respire Pink AT (Hard, Hard/Soft, EF)Respire Medical Holdings2020—
+1K223624Emerald HerbstIsland Dental Lab, Inc Dba Emerald Dental2023—
+3K214096Respire ClearRespire Medical, LLC2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199620
199710
199910
200310
200410
200510
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
201710
202020
202210
202310
FIG. 1 — Lineage of K131138, 1989–2023Source: 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
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
*K111207Respire Blue Series
Summary page 1
…ew Device 8 Identification of Legally Marketed Predicate Devices: *.Respire Pink Series - Herbst is substantially equivalent to Respire Blue Series K111207 ;SUAD K023836 in terms of intended use, indication for use, technological characteristics, performance and user…
Respire Medical2011—
*K023836The Suad Device
Summary page 1
…ication of Legally Marketed Predicate Devices: *.Respire Pink Series - Herbst is substantially equivalent to Respire Blue Series K111207 ;SUAD K023836 in terms of intended use, indication for use, technological characteristics, performance and user interface. The predic…
Strong Dental, Inc.2003—

Also cleared against K111207: 3 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K150572Respire Pink Series-Herbst-EFRespire Medical Holding20155
K170692Respire Pink Series with DentiTracRespire Medical Holding20172
K223624Emerald HerbstIsland Dental Lab, Inc Dba Emerald Dental20230
K140429Crane Acrylic Herbst ApplianceCrane Dental Laboratory, Inc.20140

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 24 years and passes through 7 companies; a new generation was cleared every 2.7 years on median.
  • None of the 16 ancestors has a recall.
  • Of its descendants, K150572 (Respire Medical Holding, 2015) has gone furthest, with 5 descendants of its own.
  • 3 other devices also cite its predicate K111207.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, 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 Respire Pink Series - Herbst Is Indicated to treat mild to moderate OSA.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131138: Respire Pink Series - Herbst.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131138

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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