510(k) Report

510(k) · Cleared

Cleared

5 Wavelength LED Facemask (TN2508)

K260598510(k) TraditionalCleared Jul 24, 2026150-day reviewClass II21 CFR 878.4810

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

iSMART Developments, Ltd. · OHS Light Based Over The Counter Wrinkle Reduction

Cleared on Jul 24, 2026 as substantially equivalent to K112362 (Silver Bay, LLC, 2012) after a 150-day review. Its family tree reaches back 2 generations to 2010.

Decided
Jul 24, 2026
Review
150 days
Class
Class II
Product code
OHS
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K101190 (2010). No later device cites it as a predicate yet.

  1. Root · 2 generations backK101190 Lightstim Anti-Wrinkle Otc Model Aal OtcLed Intellectual Properties, LLC · 2010
  2. 1 generation backK112362 C100 Wrinkle Reduction DeviceSilver Bay, LLC · 2012
  3. This deviceK260598 5 Wavelength LED Facemask (TN2508)iSMART Developments, Ltd. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K101190Lightstim Anti-Wrinkle Otc Model Aal OtcLed Intellectual Properties, LLC2010—
−1K112362C100 Wrinkle Reduction DeviceSilver Bay, LLC2012—
0 (this device)K2605985 Wavelength LED Facemask (TN2508)iSMART Developments, Ltd.2026—
FIG. 1 — Lineage of K260598, 2010–2026Source: 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 OHS? 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 OHS device

  1. #1 K223544 LED light therapy mask (FM-01, FM-02, FM-03)score 48.4 · 16 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? (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
*K112362C100 Wrinkle Reduction Device
Summary page 5
…ogy Regulation Number: 21 CFR 878.4810 Product Code: OHS Review Panel: General & Plastic Surgery Predicate Device: K112362. Light Therapy System, Quasar Calypso C100. Intended Use The 5 Wavelength LED facemask emits light in the red and near-infrare…
Silver Bay, LLC2012—

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 16 years and passes through 3 companies; a new generation was cleared every 13.9 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All OHS devices

OHS Light Based Over The Counter Wrinkle Reduction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · OHS

42in 2025

2008: 22010: 32011: 22012: 42013: 22014: 52015: 42016: 32017: 82018: 72019: 42020: 22021: 72022: 162023: 122024: 162025: 422026 (partial year): 26
2007high 42 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OHS

89in 2025

2010: 176 days median2012: 310 days median2014: 168 days median2015: 241 days median2016: 191 days median2017: 133 days median2018: 84 days median2019: 99 days median2021: 162 days median2022: 129 days median2023: 101 days median2024: 87 days median2025: 89 days median2026 (partial year): 88 days median
2007high 310 (2012) · low 84 (2018)2026

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

Recalls per year · OHS

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OHS

34in 2025

2011: 12012: 12014: 12017: 12018: 12019: 12020: 22021: 22022: 22023: 42024: 52025: 34
2007high 34 (2025) · low 0 (2007)2025

MAUDE reports naming product code OHS, 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
20082—10
20090—00
2010317600
20112—01
2012431001
20132—00
2014516801
2015424100
2016319100
2017813301
201878401
201949901
20202—02
2021716202
20221612902
20231210104
2024168705
20254289034
202626880—

What is it indicated for?

The 5 wavelength LED facemask emits light in the red and near infrared (NIR) region of the light spectrum and is indicated for the treatment of full-face wrinkles.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K260598: 5 Wavelength LED Facemask (TN2508).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K260598

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026