510(k) Report

510(k) · Cleared

Cleared

Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic Mandibular Advancement (EMA)

K203606510(k) TraditionalCleared Mar 10, 202190-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

Meris Investment Group · LRK Device, Anti-Snoring

Cleared on Mar 10, 2021 as substantially equivalent to K133683 (Microdental, Inc., 2014) and 1 other predicate after a 90-day review. Its family tree reaches back 12 generations to 1989. 3 later devices descend from it.

Decided
Mar 10, 2021
Review
90 days
Class
Class II
Product code
LRK
Recalls
None
Predicates
2

Its longest line of descent runs back 12 generations to K882303 (1989). 22 ancestors in all. 3 later devices descend from it, 2 citing it directly.

  1. Root · 12 generations backK882303 H&M Anti-Snoring DeviceHays & Meade, Inc. · 1989
  2. 8 generations between
  3. 3 generations backK161832 O2VENT TOventus Manufacturing Pty, Ltd. · 2016
  4. 2 generations backK171316 O2Vent WOventus Manufacturing Pty, Ltd. · 2017
  5. 1 generation backK190236 O2Vent OptimaOventus Manufacturing Pty, Ltd. · 2019
  6. This deviceK203606 Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep…Meris Investment Group · 2021
  7. Descendant · cites it directly · 1 of its ownK232735 EMA 3DEma Sleep Incorporated · 2024
  8. Descendant · cites it directly · 0 of its ownK252942 ShaeferHShaeferh, LLC · 2026
  9. Descendant · 2 generations on · 0 of its ownK252698 NightGuard Aire MaxNightguard Express, LLC · 2025
Show all 12 generations
  1. Root · 12 generations backK882303 H&M Anti-Snoring DeviceHays & Meade, Inc. · 1989
  2. 11 generations backK962516 Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc. · 1996
  3. 10 generations backK972061 TOAW. Keith Thornton, D.D.S. · 1997
  4. 9 generations backK022891 The Breathe EZ Anti-Snoring DeviceD&S Redhage · 2003
  5. 8 generations backK030440 Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc. · 2003
  6. 7 generations backK060388 Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with…Airway Management, Inc. · 2006
  7. 6 generations backK061732 TAP-TAirway Management, Inc. · 2006
  8. 5 generations backK103076 DynaflexDyna Flex · 2011
  9. 4 generations backK160234 OVENTOventus Manufacturing Pty, Ltd. · 2016
  10. 3 generations backK161832 O2VENT TOventus Manufacturing Pty, Ltd. · 2016
  11. 2 generations backK171316 O2Vent WOventus Manufacturing Pty, Ltd. · 2017
  12. 1 generation backK190236 O2Vent OptimaOventus Manufacturing Pty, Ltd. · 2019
  13. This deviceK203606 Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep…Meris Investment Group · 2021

Most influential descendants

Showing 3 of 3 · See all
  • K232735EMA 3DEma Sleep Incorporated · 2024 · cites it directly1descendant
  • K252942ShaeferHShaeferh, LLC · 2026 · cites it directly0descendants
  • K252698NightGuard Aire MaxNightguard Express, LLC · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K882303H&M Anti-Snoring DeviceHays & Meade, Inc.1989—
−11K962516Tap Anti-Snoring DeviceNellcor Puritan Bennett, Inc.1996—
−10K972061TOAW. Keith Thornton, D.D.S.1997—
−9K022891The Breathe EZ Anti-Snoring DeviceD&S Redhage2003—
−8K030440Oasys-Oral Airway SystemMark Abramson, D.D.S., Inc.2003—
−7K060388Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with AttachmentAirway Management, Inc.2006—
−6K061732TAP-TAirway Management, Inc.2006—
−5K103076DynaflexDyna Flex2011—
−4K160234OVENTOventus Manufacturing Pty, Ltd.2016—
−3K161832O2VENT TOventus Manufacturing Pty, Ltd.2016—
−2K171316O2Vent WOventus Manufacturing Pty, Ltd.2017—
−1K190236O2Vent OptimaOventus Manufacturing Pty, Ltd.2019—
0 (this device)K203606Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic…Meris Investment Group2021—
+1K232735EMA 3DEma Sleep Incorporated2024—
+1K252942ShaeferHShaeferh, LLC2026—
+2K252698NightGuard Aire MaxNightguard Express, LLC2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199610
199710
199910
200410
200510
200610
200710
200910
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202510
202610
FIG. 1 — Lineage of K203606, 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? (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
*K133683MICR02 Osa Device
Summary page 4
…lassification: Class 2 Predicate Devices: BůŽĐŬDĂŶĚŝďƵůĂƌĚǀĂŶĐĞŵĞŶƚ: Prosomnus MicrO2 (Primary Predicate - K133683) EůĂƐƚŝĐDĂŶĚŝďƵůĂƌĚǀĂŶĐĞŵĞŶƚ: O2Vent Optima (Reference Device Device Description:…
Microdental, Inc.2014—
*K190236O2Vent Optima
Summary page 4
…Predicate - K133683) EůĂƐƚŝĐDĂŶĚŝďƵůĂƌĚǀĂŶĐĞŵĞŶƚ: O2Vent Optima (Reference Device Device Description: - (K190236) The Serena Sleep Block Mandibular Advancement is an intraoral device that treats snoring and sleep apnea through mandibular repo…
Oventus Manufacturing Pty, Ltd.2019—
†K050592Somnomed Mas RxaSomnomed, Ltd.2005—

Also cleared against K133683: 4 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K232735EMA 3DEma Sleep Incorporated20241
K252942ShaeferHShaeferh, LLC20260

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 32 years and passes through 9 companies; a new generation was cleared every 2.1 years on median.
  • None of the 22 ancestors has a recall.
  • Of its descendants, K232735 (Ema Sleep Incorporated, 2024) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K133683.

How does its category compare?

All LRK devices

LRK Device, Anti-Snoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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 Serena Sleep Appliance is a removable medical device that is fitted in the patient’s mouth and is intended to reduce or alleviate snoring and mild to moderate obstructive sleep apnea (OSA) in adults.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K203606: Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic Mandibular Advancement (EMA).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K203606

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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