510(k) Report

510(k) · Cleared

Cleared

Nooance Led And Laser Helmet

K231321510(k) TraditionalCleared Jul 31, 202384-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

Shenzhen Kaiyan Medical Equipment Co., Ltd. · OAP Laser, Comb, Hair

Cleared on Jul 31, 2023 as substantially equivalent to K183417 (Freedom Laser Therapy, Inc., 2019) and 2 other predicates after an 84-day review. Its family tree reaches back 10 generations to 2000. 1 later device descends from it.

Decided
Jul 31, 2023
Review
84 days
Class
Class II
Product code
OAP
Recalls
None
Predicates
3

Its longest line of descent runs back 10 generations to K001179 (2000). 28 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 10 generations backK001179 Super Nova, AcubeamLight Force Therapy, Inc. · 2000
  2. 6 generations between
  3. 3 generations backK162782 iHelmet Hair Growth SystemSlinph Technologies Co., Ltd. · 2017
  4. 2 generations backK173729 Revian RedPhotonmd, Inc. · 2018
  5. 1 generation backK230336 CurrentBody Skin™ Led Hair Regrowth (Model: MZ-07)Light Tree Ventures Europe B.V. · 2023
  6. This deviceK231321 Nooance Led And Laser HelmetShenzhen Kaiyan Medical Equipment Co., Ltd. · 2023
  7. Descendant · cites it directly · 0 of its ownK262183 Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A…Shenzhen Nuon Medical Equipment Co., Ltd. · 2026
Show all 10 generations
  1. Root · 10 generations backK001179 Super Nova, AcubeamLight Force Therapy, Inc. · 2000
  2. 9 generations backK020017 Medx 1000 SeriesMedx Electronics, Inc. · 2002
  3. 8 generations backK032816 Quantum Light Therapy SystemStargate International, Inc. · 2004
  4. 7 generations backK091496 Mep-90 Hair Growth Stimulation SystemMidwest Rf, LLC · 2010
  5. 6 generations backK113097 Laser HelmetTheradome, Inc. · 2012
  6. 5 generations backK150613 LaserCap LC Pro and LC EliteTransdermal Cap, Inc. · 2015
  7. 4 generations backK153618 Capillus202Capillus, LLC · 2016
  8. 3 generations backK162782 iHelmet Hair Growth SystemSlinph Technologies Co., Ltd. · 2017
  9. 2 generations backK173729 Revian RedPhotonmd, Inc. · 2018
  10. 1 generation backK230336 CurrentBody Skin™ Led Hair Regrowth (Model: MZ-07)Light Tree Ventures Europe B.V. · 2023
  11. This deviceK231321 Nooance Led And Laser HelmetShenzhen Kaiyan Medical Equipment Co., Ltd. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K262183Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126, TK-60)Shenzhen Nuon Medical Equipment Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K001179Super Nova, AcubeamLight Force Therapy, Inc.2000—
−9K020017Medx 1000 SeriesMedx Electronics, Inc.2002—
−8K032816Quantum Light Therapy SystemStargate International, Inc.2004—
−7K091496Mep-90 Hair Growth Stimulation SystemMidwest Rf, LLC2010—
−6K113097Laser HelmetTheradome, Inc.2012—
−5K150613LaserCap LC Pro and LC EliteTransdermal Cap, Inc.2015—
−4K153618Capillus202Capillus, LLC2016—
−3K162782iHelmet Hair Growth SystemSlinph Technologies Co., Ltd.2017—
−2K173729Revian RedPhotonmd, Inc.2018—
−1K230336CurrentBody Skin™ Led Hair Regrowth (Model: MZ-07)Light Tree Ventures Europe B.V.2023—
0 (this device)K231321Nooance Led And Laser HelmetShenzhen Kaiyan Medical Equipment Co., Ltd.2023—
+1K262183Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126…Shenzhen Nuon Medical Equipment Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200710
200910
201120
201210
201310
201430
201520
201620
201710
201810
201910
202010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K231321, 2000–2026Source: 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 OAP? 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 OAP device

  1. #1 K222790 F65 Laser Systemscore 20.5 · 21 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? (3)

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
*K183417iRestore Professional 282
Summary page 5
…ore Professional 282 K231321 Page 2 of 8 510(K) Number: K183417 Review Panel: General & Plastic Surgery Product Code: OAP Regulation Number: 21 CFR 890.5500 Regulation Class: II Predicate Devi…
Freedom Laser Therapy, Inc.2019—
*K192552Irradiation Cosmetic Device
Summary page 5
…lation Class: II Predicate Device 2 Sponsor: Chongqing Peninsula Medical Technology Co., Ltd. Trade Name: Irradiation Cosmetic Device Model: HairPro Plus 510(k) Number: K192552 Common Name: Laser, Comb, Hair Classification Name: Infrared lamp Review Panel: General & Plastic Surgery Product Code: OAP Regul…
Chongqing Peninsula Medical Technology Co., Ltd.2020—
*K230336CurrentBody Skin™ Led Hair Regrowth (Model: MZ-07)
Summary page 5
….5500 Regulation Class: Class II Predicate Device 3 Sponsor: Light Tree Ventures Europe B.V. Trade Name: CurrentBody Skin™ LED Hair Regrowth Model: MZ-07 510(k) Number: K230336 Common Name: Laser, Comb, Hair Classification Name: Infrared lamp Review Panel: General & Plastic Surgery Product Code: OAP Regul…
Light Tree Ventures Europe B.V.2023—

Also cleared against K183417: 2 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
K262183Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126, TK-60)Shenzhen Nuon Medical Equipment Co., Ltd.20260

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 23 years and passes through 11 companies; a new generation was cleared every 1.7 years on median.
  • None of the 28 ancestors has a recall.
  • Of its descendants, K262183 (Shenzhen Nuon Medical Equipment Co., Ltd., 2026) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K183417.

How does its category compare?

All OAP devices

OAP Laser, Comb, Hair: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · OAP

6in 2025

2007: 12009: 12010: 12011: 42012: 22013: 32014: 32015: 82016: 82017: 52018: 152019: 92020: 92021: 52022: 82023: 82024: 102025: 62026 (partial year): 9
2007high 15 (2018) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OAP

87in 2025

2011: 89 days median2013: 262 days median2014: 80 days median2015: 126 days median2016: 83 days median2017: 83 days median2018: 87 days median2019: 89 days median2020: 88 days median2021: 89 days median2022: 99 days median2023: 81 days median2024: 94 days median2025: 87 days median2026 (partial year): 83 days median
2007high 262 (2013) · low 80 (2014)2026

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

Recalls per year · OAP

No recall names OAP since 2007.

Adverse event reports per year · OAP

11in 2025

2011: 12013: 12015: 22016: 12017: 12018: 12019: 42021: 32022: 22024: 12025: 11
2007high 11 (2025) · low 0 (2007)2025

MAUDE reports naming product code OAP, 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
20071—00
20080—00
20091—00
20101—00
201148901
20122—00
2013326201
201438000
2015812602
201688301
201758301
2018158701
201998904
202098800
202158903
202289902
202388100
2024109401
2025687011
20269830—

What is it indicated for?

The NOOĀNCE LED AND LASER HELMET is indicated to promote hair growth in males with androgenetic alopecia who have HamiltonNorwood Classifications of Ila-V and Fitzpatrick Classification of Skin Phototypes I to IV, and females with androgenetic alopecia who have Ludwig-Savin Classifications of l-II and Fitzpatrick Classification of Skin Phototypes I to IV.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231321: Nooance Led And Laser Helmet.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231321

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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