510(k) Report

510(k) · Cleared

Cleared

The Luco Hybrid OSA Appliance

K160477510(k) TraditionalCleared Jul 29, 2016161-day reviewClass U

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Luco Hybrid Osa Appliance, Inc. · OCO Mouthguard, Migraine/Tension Headache

Cleared on Jul 29, 2016 after a 161-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
Jul 29, 2016
Review
161 days
Class
Class U
Product code
OCO
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2024: 1 descendant cleared201620182020202220242026
  1. This deviceK160477 The Luco Hybrid OSA ApplianceLuco Hybrid Osa Appliance, Inc. · 2016
  2. Descendant · cites it directly · 0 of its ownK240463 Slow Wave DS8 (SWDS802)Slow Wave, Inc. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K240463Slow Wave DS8 (SWDS802)Slow Wave, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K160477The Luco Hybrid OSA ApplianceLuco Hybrid Osa Appliance, Inc.2016—
+1K240463Slow Wave DS8 (SWDS802)Slow Wave, Inc.2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K160477, 2016–2024Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in OCO? 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 OCO device

  1. #1 K202523 TMJ Relaxscore 1.6 · 1 generation · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K240463Slow Wave DS8 (SWDS802)Slow Wave, Inc.20240

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?

  • Of its descendants, K240463 (Slow Wave, Inc., 2024) has gone furthest, with 0 descendants of its own.

How does its category compare?

All OCO devices

OCO Mouthguard, Migraine/Tension Headache: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · OCO

1in 2021

2016: 12021: 1
2007high 1 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OCO

Too few OCO 510(k)s in any year since 2007 to give a median.

Recalls per year · OCO

No recall names OCO since 2007.

Adverse event reports per year · OCO

5in 2023

2010: 12013: 12015: 12021: 22023: 5
2007high 5 (2023) · low 0 (2007)2025

MAUDE reports naming product code OCO, 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
20070—00
20080—00
20090—00
20100—01
20110—00
20120—00
20130—01
20140—00
20150—01
20161—00
20170—00
20180—00
20190—00
20200—00
20211—02
20220—00
20230—05
20240—00
20250—00
20260—0—

What is it indicated for?

1. A device to be used for the treatment of sleep bruxism and

2. As an aid in the treatment of associated tension/migraine type headaches in adults.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K160477: The Luco Hybrid OSA Appliance.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K160477

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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