510(k) Report

510(k) · Cleared

Cleared

Varaya AR , Varaya Sport

K112494510(k) TraditionalCleared May 16, 2012261-day reviewClass II21 CFR 890.5500

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

Varaya Photoceuticals, LLC · ILY Lamp, Infrared, Therapeutic Heating

Cleared on May 16, 2012 as substantially equivalent to K032229 (Quantum Devices, Inc., 2003) and 3 other predicates after a 261-day review. Its family tree reaches back 3 generations to 2000. 1 later device descends from it.

Decided
May 16, 2012
Review
261 days
Class
Class II
Product code
ILY
Recalls
None
Predicates
4

Its longest line of descent runs back 3 generations to K001179 (2000). 11 ancestors in all, the oldest K974468 (1998). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2003: 1 other ancestor1998: 2 other ancestors2008: 1 other ancestor2007: 1 other ancestor2002: 1 other ancestor2000: 1 other ancestor2015: 1 descendant clearedK001179 · Super Nova, Acubeam · Light Force Therapy, Inc. · 2000K020017 · Medx 1000 Series · Medx Electronics, Inc. · 2002K090008 · Tanda Restore, Model Ptscs · Pharos Life Corporation · 20091995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 4 other ancestors3 generations back: 1 other ancestor 1 generation forward: 1 descendant K090008 · Tanda Restore, Model Ptscs · Pharos Life Corporation · 2009K020017 · Medx 1000 Series · Medx Electronics, Inc. · 2002K001179 · Super Nova, Acubeam · Light Force Therapy, Inc. · 20000
  1. Root · 3 generations backK001179 Super Nova, AcubeamLight Force Therapy, Inc. · 2000
  2. 2 generations backK020017 Medx 1000 SeriesMedx Electronics, Inc. · 2002
  3. 1 generation backK090008 Tanda Restore, Model PtscsPharos Life Corporation · 2009
  4. This deviceK112494 Varaya AR , Varaya SportVaraya Photoceuticals, LLC · 2012
  5. Descendant · cites it directly · 0 of its ownK150716 Varaya SportVaraya Photoceuticals, LLC · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K150716Varaya SportVaraya Photoceuticals, LLC · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K001179Super Nova, AcubeamLight Force Therapy, Inc.2000—
−2K020017Medx 1000 SeriesMedx Electronics, Inc.2002—
−1K090008Tanda Restore, Model PtscsPharos Life Corporation2009—
0 (this device)K112494Varaya AR , Varaya SportVaraya Photoceuticals, LLC2012—
+1K150716Varaya SportVaraya Photoceuticals, LLC2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199820
200010
200210
200310
200710
200810
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of K112494, 2000–2015Source: 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 ILY? 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 ILY device

  1. #1 K242755 Medical Diode Laser Systems (VELAS II-30B…score 18.7 · 22 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? (4)

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
*K032229Quantum Warp 10 Light Delivery System
Summary page 1
…Panel: Physical Medicine Product Code: ILY Regulation No.: 890.5500 3. Predicate Devices: Warp 10 (K032229), Tanda Pro Restore (K090008), Diomedics PainX 2000 Model 900 ([K982546), RXLight ([K100213).…
Quantum Devices, Inc.2003—
*K090008Tanda Restore, Model Ptscs
Summary page 1
…dicine Product Code: ILY Regulation No.: 890.5500 3. Predicate Devices: Warp 10 (K032229), Tanda Pro Restore (K090008), Diomedics PainX 2000 Model 900 ([K982546), RXLight ([K100213).…
Pharos Life Corporation2009—
*K982546Phaser-2000
Summary page 1
…Regulation No.: 890.5500 3. Predicate Devices: Warp 10 (K032229), Tanda Pro Restore (K090008), Diomedics PainX 2000 Model 900 ([K982546), RXLight ([K100213). '7 === Page 2…
Diomedics, Inc.1998—
*K100213Lumanosity Celebrity, Model 204
Summary page 1
…890.5500 3. Predicate Devices: Warp 10 (K032229), Tanda Pro Restore (K090008), Diomedics PainX 2000 Model 900 ([K982546), RXLight ([K100213). '7 4. Device Des…
Lumanosity, Inc.2010—

Also cleared against K032229: 14 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
K150716Varaya SportVaraya Photoceuticals, LLC20150

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 12 years and passes through 4 companies; a new generation was cleared every 2.6 years on median.
  • None of the 11 ancestors has a recall.
  • Of its descendants, K150716 (Varaya Photoceuticals, LLC, 2015) has gone furthest, with 0 descendants of its own.
  • 14 other devices also cite its predicate K032229.

How does its category compare?

All ILY devices

ILY Lamp, Infrared, Therapeutic Heating: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · ILY

1in 2025

2007: 102008: 162009: 132010: 82011: 92012: 112013: 92014: 112015: 112016: 82017: 52020: 12022: 22023: 12024: 12025: 12026 (partial year): 1
2007high 16 (2008) · low 0 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ILY

116in 2017

2007: 128 days median2008: 165 days median2009: 189 days median2010: 185 days median2011: 198 days median2012: 130 days median2013: 211 days median2014: 153 days median2015: 146 days median2016: 214 days median2017: 116 days median
2007high 214 (2016) · low 116 (2017)2026

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

Recalls per year · ILY

1in 2025

2010: 12012: 32022: 42023: 12025: 12026 (partial year): 1
2007high 4 (2022) · low 0 (2007)2026

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

Adverse event reports per year · ILY

17in 2025

2007: 242008: 202009: 92010: 72011: 102012: 72013: 82015: 22016: 22017: 122018: 12019: 72020: 52021: 52022: 22023: 152024: 192025: 17
2007high 24 (2007) · low 0 (2014)2025

MAUDE reports naming product code ILY, 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
200710128024
200816165020
20091318909
2010818517
20119198010
20121113037
2013921108
20141115300
20151114602
2016821402
20175116012
20180—01
20190—07
20201—05
20210—05
20222—42
20231—115
20241—019
20251—117
20261—1—

What is it indicated for?

The Varaya Sport Model 200 is indicated/intended for the temporary relief of minor muscle and joint pain, arthritis and muscle spasm; promoting the relaxation of muscle tissue; and to temporarily increase local blood circulation where applied.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112494: Varaya AR , Varaya Sport.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K112494

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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