510(k) Report

510(k) · Cleared

Cleared

Hair Up

K180617510(k) TraditionalCleared Jun 1, 201885-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

Y & J Bio Co., Ltd. · OAP Laser, Comb, Hair

Cleared on Jun 1, 2018 as substantially equivalent to K140931 (Apira Science, Inc., 2014) after an 85-day review. Its family tree reaches back 2 generations to 2012. 1 later device descends from it.

Decided
Jun 1, 2018
Review
85 days
Class
Class II
Product code
OAP
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K122248 (2012). 1 later device descends from it, 1 citing it directly.

Descendants, by generation 1 generation forward: 1 descendant K140931 · Igrow II Hair Growth System · Apira Science, Inc. · 2014K122248 · Igrow II Hair Growth System · Apira Science, Inc. · 20120
  1. Root · 2 generations backK122248 Igrow II Hair Growth SystemApira Science, Inc. · 2012
  2. 1 generation backK140931 Igrow II Hair Growth SystemApira Science, Inc. · 2014
  3. This deviceK180617 Hair UpY & J Bio Co., Ltd. · 2018
  4. Descendant · cites it directly · 0 of its ownK202983 easy HairfullY & J Bio Co., Ltd. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K202983easy HairfullY & J Bio Co., Ltd. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K122248Igrow II Hair Growth SystemApira Science, Inc.2012—
−1K140931Igrow II Hair Growth SystemApira Science, Inc.2014—
0 (this device)K180617Hair UpY & J Bio Co., Ltd.2018—
+1K202983easy HairfullY & J Bio Co., Ltd.2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K180617, 2012–2020Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K140931Igrow II Hair Growth System
Summary page 4
…evice Table 5.1 Primary Predicate device Applicant Device Name 510(k) Number Apira Science Inc. iGrow-II Hair Growth System K140931 Table 5.2 References predicate devices Applicant Device Name 510(k) Number Apira Science Inc…
Apira Science, Inc.2014—
†K141567Igrow - II Hair Growth System, Igrow Hair Growth SystemApira Science, Inc.2014—
†K162782iHelmet Hair Growth SystemSlinph Technologies Co., Ltd.2017—

Also cleared against K140931: 6 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
K202983easy HairfullY & J Bio Co., Ltd.20200

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 6 years and passes through 2 companies; a new generation was cleared every 3.5 years on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K202983 (Y & J Bio Co., Ltd., 2020) has gone furthest, with 0 descendants of its own.
  • 6 other devices also cite its predicate K140931.

How does its category compare?

All OAP devices

OAP Laser, Comb, Hair: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, 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 Hair Up is intended to promote hair growth in males with androgenetic alopecia who have Norwood Hamilton Classifications of IIa to V and Fitzpatrick Classification of Skin Phototypes I to IV, and in females with androgenetic alopecia who have Ludwig-Savin Classifications of I-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. “K180617: Hair Up.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K180617

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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