510(k) Report

510(k) · Cleared

Cleared

SleepRight ProRx Custom Dental Guard

K172223510(k) TraditionalCleared Nov 17, 2017116-day reviewClass U

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

Splintek, Inc. · OBR Mouthguard, Over-The-Counter

Cleared on Nov 17, 2017 as substantially equivalent to K121272 (Akervall Technologies, Inc., 2012) and 1 other predicate after a 116-day review. Its family tree reaches back 3 generations to 2003. 3 later devices descend from it.

Decided
Nov 17, 2017
Review
116 days
Class
Class U
Product code
OBR
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K022809 (2003). 8 ancestors in all, the oldest K010876 (2001). 3 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 2 other ancestors2006: 1 other ancestor2001: 1 other ancestor2020: 1 descendant cleared2021: 1 descendant cleared2025: 1 descendant clearedK022809 · EZ Splint & EZ Splint PM · Power Products, Inc.-Splintek · 2003K072147 · Den Tek Comfort Fit Nightguard · Den Tek Oral Care, Inc. · 2007K121272 · Protech Dent · Akervall Technologies, Inc. · 2012200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 3 other ancestors 1 generation forward: 2 descendants2 generations forward: 1 descendant K121272 · Protech Dent · Akervall Technologies, Inc. · 2012K072147 · Den Tek Comfort Fit Nightguard · Den Tek Oral Care, Inc. · 2007K022809 · EZ Splint & EZ Splint PM · Power Products, Inc.-Splintek · 20030
  1. Root · 3 generations backK022809 EZ Splint & EZ Splint PMPower Products, Inc.-Splintek · 2003
  2. 2 generations backK072147 Den Tek Comfort Fit NightguardDen Tek Oral Care, Inc. · 2007
  3. 1 generation backK121272 Protech DentAkervall Technologies, Inc. · 2012
  4. This deviceK172223 SleepRight ProRx Custom Dental GuardSplintek, Inc. · 2017
  5. Descendant · cites it directly · 2 of its ownK193577 SleepRight ProRx Custom Dental GuardSplintek, Inc. · 2020
  6. Descendant · 2 generations on · 0 of its ownK250743 Remvia NightGuardRemvia · 2025
  7. Descendant · cites it directly · 0 of its ownK212706 SleepRight ProRx + Custom Dental Guard, SleepRight ProRx Custom…Splintek, Inc. · 2021

Most influential descendants

Showing 3 of 3 · See all
  • K193577SleepRight ProRx Custom Dental GuardSplintek, Inc. · 2020 · cites it directly2descendants
  • K250743Remvia NightGuardRemvia · 2025 · 2 generations on0descendants
  • K212706SleepRight ProRx + Custom Dental Guard, SleepRight ProRx Custom Dental GuardSplintek, Inc. · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K022809EZ Splint & EZ Splint PMPower Products, Inc.-Splintek2003—
−2K072147Den Tek Comfort Fit NightguardDen Tek Oral Care, Inc.2007—
−1K121272Protech DentAkervall Technologies, Inc.2012—
0 (this device)K172223SleepRight ProRx Custom Dental GuardSplintek, Inc.2017—
+1K193577SleepRight ProRx Custom Dental GuardSplintek, Inc.2020—
+2K250743Remvia NightGuardRemvia2025—
+1K212706SleepRight ProRx + Custom Dental Guard, SleepRight ProRx Custom Dental GuardSplintek, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200610
200720

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
202510
FIG. 1 — Lineage of K172223, 2003–2025Source: 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 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? (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
*K121272Protech Dent
Summary page 5
…: Mouthguard Classification Name: Unclassified (OBR, MQC) C. Primary Predicate Device: ProTech Dent® (Akervall Technologies, K121272) Reference Predicate Device: SleepRight® -Advance (Splintek Inc., K071404) D. Device Description: The SleepRigh…
Akervall Technologies, Inc.2012—
*K071404Sleep Right - Select, Low Profile and Advance
Summary page 5
…(OBR, MQC) C. Primary Predicate Device: ProTech Dent® (Akervall Technologies, K121272) Reference Predicate Device: SleepRight® -Advance (Splintek Inc., K071404) D. Device Description: The SleepRight® ProRx® Custom Dental Guard is a full occlusal custom formable protector tha…
Power Products, Inc.-Splintek2007—

Also cleared against K121272: 2 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
K193577SleepRight ProRx Custom Dental GuardSplintek, Inc.20202
K212706SleepRight ProRx + Custom Dental Guard, SleepRight ProRx Custom Dental GuardSplintek, Inc.20210

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 14 years and passes through 4 companies; a new generation was cleared every 5.1 years on median.
  • None of the 8 ancestors has a recall.
  • Of its descendants, K193577 (Splintek, Inc., 2020) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K121272.

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. 2017, 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?

The SleepRight® ProRx® Custom Dental Guard is indicated for the protection against bruxism or nighttime teeth grinding. It is intended to reduce damage to the teeth and to prevent the noise associated with bruxing or grinding.

Protection against teeth grinding, bruxism and jaw clenching.

Short-term pain relief from muscle spasm due to occlusal interference.

For the prevention of chronic tension and temporomandibular joint (TMJ)

syndrome that is caused by chronic jaw clenching of the mandibular and maxillary teeth by the temporalis muscle.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K172223: SleepRight ProRx Custom Dental Guard.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172223

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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