510(k) Report

510(k) · Cleared

Cleared

NTI ClenchGuard

K211158510(k) TraditionalCleared Sep 17, 2021151-day reviewClass U

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

Boyd Research, Inc. · OBR Mouthguard, Over-The-Counter

Cleared on Sep 17, 2021 after a 151-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 2 later devices descend from it.

Decided
Sep 17, 2021
Review
151 days
Class
Class U
Product code
OBR
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2026: 1 descendant cleared2025: 1 descendant cleared2020202220242026
  1. This deviceK211158 NTI ClenchGuardBoyd Research, Inc. · 2021
  2. Descendant · cites it directly · 1 of its ownK251778 Remi Custom Night GuardRemi · 2025
  3. Descendant · cites it directly · 0 of its ownK253641 Owl Night GuardOwl Dental Lab, Inc. · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K251778Remi Custom Night GuardRemi · 2025 · cites it directly1descendant
  • K253641Owl Night GuardOwl Dental Lab, Inc. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K211158NTI ClenchGuardBoyd Research, Inc.2021—
+1K251778Remi Custom Night GuardRemi2025—
+1K253641Owl Night GuardOwl Dental Lab, Inc.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
202610
FIG. 1 — Lineage of K211158, 2021–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 OBR? 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 OBR device

  1. #1 K251778 Remi Custom Night Guardscore 15.6 · 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?

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

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K251778Remi Custom Night GuardRemi20251
K253641Owl Night GuardOwl Dental Lab, Inc.20260

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, K251778 (Remi, 2025) has gone furthest, with 1 descendant of its own.

How does its category compare?

All OBR devices

OBR Mouthguard, Over-The-Counter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · OBR

3in 2025

2007: 22008: 52009: 32010: 22011: 12012: 42013: 22014: 22015: 12016: 12017: 12018: 22019: 32020: 32021: 22022: 22023: 12024: 22025: 32026 (partial year): 4
2007high 5 (2008) · low 1 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OBR

129in 2025

2008: 55 days median2009: 16 days median2012: 145 days median2019: 266 days median2020: 161 days median2025: 129 days median2026 (partial year): 103 days median
2007high 266 (2019) · low 16 (2009)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · OBR

No recall names OBR since 2007.

Adverse event reports per year · OBR

13in 2025

2007: 12009: 72010: 32012: 42013: 82014: 7762015: 312016: 162017: 242018: 232019: 292020: 152021: 102022: 62023: 52024: 182025: 13
2007high 776 (2014) · low 0 (2008)2025

MAUDE reports naming product code OBR, 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
20072—01
200855500
200931607
20102—03
20111—00
2012414504
20132—08
20142—0776
20151—031
20161—016
20171—024
20182—023
20193266029
20203161015
20212—010
20222—06
20231—05
20242—018
20253129013
202641030—

What is it indicated for?

1. As an aid in the reduction of medically diagnosed migraine pain associated with jaw clenching and bruxing;

2. Protection against bruxism or nighttime teeth grinding and reduce damage and the noise associated with bruxing and/or grinding.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K211158: NTI ClenchGuard.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211158

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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