510(k) Report

510(k) · Cleared

Cleared

Crane Acrylic Herbst Appliance

K140429510(k) TraditionalCleared Sep 11, 2014204-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

Crane Dental Laboratory, Inc. · LRK Device, Anti-Snoring

Cleared on Sep 11, 2014 as substantially equivalent to K131138 (Respire Medical, 2013) after a 204-day review. Its family tree reaches back 8 generations to 1989.

Decided
Sep 11, 2014
Review
204 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K882303 (1989). 17 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK882303 H&M Anti-Snoring DeviceHays & Meade, Inc. · 1989
  2. 7 generations backK962516 Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc. · 1996
  3. 6 generations backK972061 TOAW. Keith Thornton, D.D.S. · 1997
  4. 5 generations backK022891 The Breathe EZ Anti-Snoring DeviceD&S Redhage · 2003
  5. 4 generations backK030440 Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc. · 2003
  6. 3 generations backK060388 Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with…Airway Management, Inc. · 2006
  7. 2 generations backK111207 Respire Blue SeriesRespire Medical · 2011
  8. 1 generation backK131138 Respire Pink Series - HerbstRespire Medical · 2013
  9. This deviceK140429 Crane Acrylic Herbst ApplianceCrane Dental Laboratory, Inc. · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K882303H&M Anti-Snoring DeviceHays & Meade, Inc.1989—
−7K962516Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc.1996—
−6K972061TOAW. Keith Thornton, D.D.S.1997—
−5K022891The Breathe EZ Anti-Snoring DeviceD&S Redhage2003—
−4K030440Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc.2003—
−3K060388Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with AttachmentAirway Management, Inc.2006—
−2K111207Respire Blue SeriesRespire Medical2011—
−1K131138Respire Pink Series - HerbstRespire Medical2013—
0 (this device)K140429Crane Acrylic Herbst ApplianceCrane Dental Laboratory, Inc.2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199620
199710
199910
200310
200410
200510
200810
FIG. 1 — Lineage of K140429, 1989–2014Source: 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
*K131138Respire Pink Series - Herbst
Summary page 4
…Device Class‐ II Substantial Equivalence is claimed to this Predicate Device:  Respire Medical LLC‐ Respire Pink Series (K131138) Device Description: The Crane Acrylic Herbst Appliance is comprised of upper and lower patient‐specific acrylic splints connec…
Respire Medical2013—

Also cleared against K131138: 3 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 25 years and passes through 8 companies; a new generation was cleared every 2.7 years on median.
  • None of the 17 ancestors has a recall.
  • 3 other devices also cite its predicate K131138.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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 Crane Acrylic Herbst Appliance is intended for use in patients 18 years of age or older for the reduction of night time snoring and mild to moderate obstructive sleep apnea.

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. “K140429: Crane Acrylic Herbst Appliance.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140429

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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