510(k) Report

510(k) · Cleared

Cleared

Neuhat Hair Growth System; ibeauty.com Laser Cap

K231153510(k) TraditionalCleared Jun 23, 202360-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

Nature, Inc.redible, Inc. · OAP Laser, Comb, Hair

Cleared on Jun 23, 2023 as substantially equivalent to K210169 (Dongguan Lescolton Intelligent Electrical Appliance Co., Ltd., 2021) after a 60-day review. Its family tree reaches back 8 generations to 2007. 1 later device descends from it.

Decided
Jun 23, 2023
Review
60 days
Class
Class II
Product code
OAP
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K060305 (2007). 14 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 8 generations backK060305 Hairmax LasercombLexington International, LLC · 2007
  2. 7 generations backK093499 Hairmax LasercombLexington International, LLC · 2009
  3. 6 generations backK103368 Hairmax LasercombLexington International, LLC · 2011
  4. 5 generations backK142573 HairMax LaserComb, HairMax LaserCombLexington International, LLC · 2014
  5. 4 generations backK160285 Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC · 2016
  6. 3 generations backK162071 IllumiFlow Laser CapEglobal, LLC · 2017
  7. 2 generations backK200464 LG Pra. L Derma LD Scalp CareLg Electronics.Inc · 2020
  8. 1 generation backK210169 Hair Growth DeviceDongguan Lescolton Intelligent Electrical Appliance Co., Ltd. · 2021
  9. This deviceK231153 Neuhat Hair Growth System; ibeauty.com Laser CapNature, Inc.redible, Inc. · 2023
  10. Descendant · cites it directly · 0 of its ownK251017 CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)Shenzhen Kaiyan Medical Equipment Co., Ltd. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K251017CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)Shenzhen Kaiyan Medical Equipment Co., Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K060305Hairmax LasercombLexington International, LLC2007—
−7K093499Hairmax LasercombLexington International, LLC2009—
−6K103368Hairmax LasercombLexington International, LLC2011—
−5K142573HairMax LaserComb, HairMax LaserCombLexington International, LLC2014—
−4K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC2016—
−3K162071IllumiFlow Laser CapEglobal, LLC2017—
−2K200464LG Pra. L Derma LD Scalp CareLg Electronics.Inc2020—
−1K210169Hair Growth DeviceDongguan Lescolton Intelligent Electrical Appliance Co., Ltd.2021—
0 (this device)K231153Neuhat Hair Growth System; ibeauty.com Laser CapNature, Inc.redible, Inc.2023—
+1K251017CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)Shenzhen Kaiyan Medical Equipment Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201420
201510
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K231153, 2007–2025Source: 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? (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
*K210169Hair Growth Device
Summary page 4
…Applicant Primary Predicate Reference device Device 510(k) Number K210169 K200464 Trade name Hair Growth Device LG Pra.L Derma LD…
Dongguan Lescolton Intelligent Electrical Appliance Co., Ltd.2021—
†K200464LG Pra. L Derma LD Scalp CareLg Electronics.Inc2020—

Also cleared against K210169: 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
K251017CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)Shenzhen Kaiyan Medical Equipment Co., Ltd.20250

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 6 companies; a new generation was cleared every 2.2 years on median.
  • None of the 14 ancestors has a recall.
  • Of its descendants, K251017 (Shenzhen Kaiyan Medical Equipment Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K210169.

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?

Neuhat Hair Growth System is indicated to promote hair growth in males with androgenic alopecia who have Norwood-Hamilton classifications of IIa-V and females with androgenic alopecia who have Ludwig-Savin Classifications of I-II and Fitzpatrick Classification of Skin Phototypes I-IV.

ibeauty.com Laser Cap is indicated to promote hair growth in males with androgenic alopecia who have Norwood-Hamilton classifications of IIa-V and females with androgenic alopecia who have Ludwig-Savin Classifications of I-II and Fitzpatrick Classification of Skin Phototypes I-IV.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231153: Neuhat Hair Growth System; ibeauty.com Laser Cap.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231153

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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