510(k) Report

510(k) · Cleared

Cleared

Star-Lite -LM, Model SL8809

K092460510(k) TraditionalCleared Mar 5, 2010206-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

Ps Advanced Engineering · OHS Light Based Over The Counter Wrinkle Reduction

Cleared on Mar 5, 2010 as substantially equivalent to K072459 (Photo Therapeutics, Inc., 2008) after a 206-day review. Its family tree reaches back 11 generations to 1995. 1 later device descends from it.

Decided
Mar 5, 2010
Review
206 days
Class
Class II
Product code
OHS
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K943450 (1995). 91 ancestors in all, the oldest K800617 (1980). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2003: 1 other ancestor2002: 3 other ancestors2000: 6 other ancestors1998: 10 other ancestors2001: 1 other ancestor1999: 4 other ancestors1996: 12 other ancestors1995: 9 other ancestors1997: 13 other ancestors1994: 8 other ancestors1993: 3 other ancestors1991: 3 other ancestors1990: 1 other ancestor1980: 1 other ancestor1992: 3 other ancestors1985: 1 other ancestor2014: 1 descendant clearedK943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995×2: 2 generations cleared close together, K961069 (1996), K962445 (1996) ×2: 2 generations cleared close together, K964849 (1997), K971532 (1997) K974521 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1998K982816 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1999K022266 · Aurora SR · Syneron Medical, Ltd. · 2002K030426 · Omnilux Red · Photo Therapeutics Limited · 2003K050216 · Omnilux Revive and Omnilux Plus · Photo Therapeutics Limited · 2005K072459 · Omnilux New-U · Photo Therapeutics, Inc. · 200819801990200020102020
  1. Root · 11 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 7 generations between
  3. 3 generations backK030426 Omnilux RedPhoto Therapeutics Limited · 2003
  4. 2 generations backK050216 Omnilux Revive and Omnilux PlusPhoto Therapeutics Limited · 2005
  5. 1 generation backK072459 Omnilux New-UPhoto Therapeutics, Inc. · 2008
  6. This deviceK092460 Star-Lite -LM, Model SL8809Ps Advanced Engineering · 2010
  7. Descendant · cites it directly · 0 of its ownK133546 Starlite-OM, Light Effects, ThibiantPs Advanced Engineering · 2014
Show all 11 generations
  1. Root · 11 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 10 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 9 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 8 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 7 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
  6. 6 generations backK974521 Vnus Closure SystemVnus Medical Technologies, Inc. · 1998
  7. 5 generations backK982816 Vnus Closure SystemVnus Medical Technologies, Inc. · 1999
  8. 4 generations backK022266 Aurora SRSyneron Medical, Ltd. · 2002
  9. 3 generations backK030426 Omnilux RedPhoto Therapeutics Limited · 2003
  10. 2 generations backK050216 Omnilux Revive and Omnilux PlusPhoto Therapeutics Limited · 2005
  11. 1 generation backK072459 Omnilux New-UPhoto Therapeutics, Inc. · 2008
  12. This deviceK092460 Star-Lite -LM, Model SL8809Ps Advanced Engineering · 2010

Most influential descendants

Showing 1 of 1 · See all
  • K133546Starlite-OM, Light Effects, ThibiantPs Advanced Engineering · 2014 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−10K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−9K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−8K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−7K971532Arthrocare Electrosurgery SystemArthrocare Corp.1997—
−6K974521Vnus Closure SystemVnus Medical Technologies, Inc.1998—
−5K982816Vnus Closure SystemVnus Medical Technologies, Inc.1999—
−4K022266Aurora SRSyneron Medical, Ltd.2002—
−3K030426Omnilux RedPhoto Therapeutics Limited2003—
−2K050216Omnilux Revive and Omnilux PlusPhoto Therapeutics Limited2005—
−1K072459Omnilux New-UPhoto Therapeutics, Inc.2008—
0 (this device)K092460Star-Lite -LM, Model SL8809Ps Advanced Engineering2010—
+1K133546Starlite-OM, Light Effects, ThibiantPs Advanced Engineering2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198510
199010
199130
199230
199330
199480
199590
1996120
1997130
1998100
199940
200060
200110
200230
200310
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
FIG. 1 — Lineage of K092460, 1995–2014Source: 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
Get a 510(k) Report

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
*K072459Omnilux New-U
Summary page 2
…for Over The Counter use, the manufacturer believes this is the classification name which is most applicable. 3) Predicate Device Omnilux New-U (K072459) 4) Device Description Starl-ite-LM is a handheld ergonomically designed ABS plastic housed device with a locking Med…
Photo Therapeutics, Inc.2008—

Also cleared against K072459: 5 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K133546Starlite-OM, Light Effects, ThibiantPs Advanced Engineering20140

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 15 years and passes through 6 companies; a new generation was cleared every 1.1 years on median.
  • 3 of the 91 ancestors have a recall of any class.
  • Of its descendants, K133546 (Ps Advanced Engineering, 2014) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K072459.

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. 2010, 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 StarLite-LM is a hand held device intended for over the counter (OTC) patient usage to specifically treat periorbital wrinkles. The target patient population is identical to that of the predicate device. StarLite-LM emits LED light energy in the red and infrared spectrum.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092460: Star-Lite -LM, Model SL8809.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K092460

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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