510(k) Report

510(k) · Cleared

Cleared

Dental Pain Eraser

K193570510(k) SpecialCleared Jan 17, 202025-day reviewClass U

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

Synapse Dental · LWM Device, Electrical Dental Anesthesia

Cleared on Jan 17, 2020 as substantially equivalent to K182947 (Synapse Dental, LLC, 2019) after a 25-day review. Its family tree reaches back 2 generations to 1992.

Decided
Jan 17, 2020
Review
25 days
Class
Class U
Product code
LWM
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K915717 (1992). No later device cites it as a predicate yet.

K915717 · Cedeta · D-W Intl. · 1992K182947 · Dental Pain Eraser · Synapse Dental, LLC · 20191990199520002005201020152020
  1. Root · 2 generations backK915717 CedetaD-W Intl. · 1992
  2. 1 generation backK182947 Dental Pain EraserSynapse Dental, LLC · 2019
  3. This deviceK193570 Dental Pain EraserSynapse Dental · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K915717CedetaD-W Intl.1992—
−1K182947Dental Pain EraserSynapse Dental, LLC2019—
0 (this device)K193570Dental Pain EraserSynapse Dental2020—
FIG. 1 — Lineage of K193570, 1992–2020Source: 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 LWM? 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 LWM device

  1. #1 K192429 Dental Pain Eraserscore -1.0 · 2 generations · no Class I recall
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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
*K182947Dental Pain Eraser
Summary page 3
…LWM Trade Name: Dental Pain Eraser DPE-C300 Generic/Common Name: Device, Electrical Dental Anesthesia PREDICATE DEVICE(S) [807.92(a)(3)] Dental Pain Eraser DPE-C300 (K182947) DEVICE DESCRIPTION [807.92(a)(4)] The Dental Pain Eraser DPE-C300 is a non-invasive electrical stimulation device that is used…
Synapse Dental, LLC2019—

Also cleared against K182947: 1 other device →

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 28 years and passes through 3 companies; a new generation was cleared every 26.3 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K182947.

How does its category compare?

All LWM devices

LWM Device, Electrical Dental Anesthesia: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · LWM

2in 2020

2019: 12020: 2
2007high 2 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LWM

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

Recalls per year · LWM

No recall names LWM since 2007.

Adverse event reports per year · LWM

No MAUDE report names LWM since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20191—00
20202—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The Dental Pain Eraser DPE-C300 is intended to provide temporary dental anesthesia (pain relief) and is indicated for use before, during, or after dental and orthodontic procedures, and other sources of oral pain. It is intended for use by dental/orthodontic professionals for the alleviation of oral pain.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K193570: Dental Pain Eraser.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K193570

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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