510(k) Report

510(k) · Cleared

Cleared

Grivamax Family of Lasers, Models 272 and 148

K211192510(k) TraditionalCleared Jul 20, 202190-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

Leana Orders, Inc. · OAP Laser, Comb, Hair

Cleared on Jul 20, 2021 as substantially equivalent to K173678 (Cosmo Far East Technology Limited, 2018) and 1 other predicate after a 90-day review. Its family tree reaches back 7 generations to 2007.

Decided
Jul 20, 2021
Review
90 days
Class
Class II
Product code
OAP
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K060305 (2007). 14 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK060305 Hairmax LasercombLexington International, LLC · 2007
  2. 6 generations backK093499 Hairmax LasercombLexington International, LLC · 2009
  3. 5 generations backK103368 Hairmax LasercombLexington International, LLC · 2011
  4. 4 generations backK142573 HairMax LaserComb, HairMax LaserCombLexington International, LLC · 2014
  5. 3 generations backK160285 Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC · 2016
  6. 2 generations backK162071 IllumiFlow Laser CapEglobal, LLC · 2017
  7. 1 generation backK171895 Grivamax Hair Growth SystemLeana Orders, Inc. · 2017
  8. This deviceK211192 Grivamax Family of Lasers, Models 272 and 148Leana Orders, Inc. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K060305Hairmax LasercombLexington International, LLC2007—
−6K093499Hairmax LasercombLexington International, LLC2009—
−5K103368Hairmax LasercombLexington International, LLC2011—
−4K142573HairMax LaserComb, HairMax LaserCombLexington International, LLC2014—
−3K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC2016—
−2K162071IllumiFlow Laser CapEglobal, LLC2017—
−1K171895Grivamax Hair Growth SystemLeana Orders, Inc.2017—
0 (this device)K211192Grivamax Family of Lasers, Models 272 and 148Leana Orders, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201420
201510
201710
201810
FIG. 1 — Lineage of K211192, 2007–2021Source: 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
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What was it cleared against? (2)

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
*K173678Diode Laser Cap
Summary page 5
…lassification Code: OAP (Laser, comb, hair) Predicate Devices: Device Trade Name Manufacturer Diode Laser Cap (K173678) Cosmo Far East Technology Limited Grivamax Hair Growth System (K171895) Cosmo Far East…
Cosmo Far East Technology Limited2018—
*K171895Grivamax Hair Growth System
Summary page 5
…Manufacturer Diode Laser Cap (K173678) Cosmo Far East Technology Limited Grivamax Hair Growth System (K171895) Cosmo Far East Technology Limited Reference Devices: None…
Leana Orders, Inc.2017—

Also cleared against K173678: 6 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 14 years and passes through 4 companies; a new generation was cleared every 1.4 years on median.
  • None of the 14 ancestors has a recall.
  • 6 other devices also cite its predicate K173678.

How does its category compare?

All OAP devices

OAP Laser, Comb, Hair: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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 Grivamax Family of Lasers , Models 272 and 148 are indicated to promote hair growth in females with androgenetic alopecia who have Ludwig-Savin Classifications of I - II, males who have Norwood-Hamilton Classifications of Ila - V and for both, Fitzpatrick Classification of Skin Phototypes I to IV.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211192: Grivamax Family of Lasers, Models 272 and 148.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K211192

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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