510(k) Report

FDA product code · General and plastic surgery

Light Based Over-The-Counter Hair Removal

OHTClass II21 CFR 878.4810510(k) required167 decisions since 20060 recalls

167 FDA decisions since 2006. 510(k) reviews decided 2021–2025 took a median of 82 days (half between 57 and 90). No recall names this code. The most-cited predicate is K160968, named by 27 later devices.

Over-the-counter device uses thermal energy to kill hair follicles for hair removal.

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

FIG. A — Illustration, general and plastic surgery panel

Twenty years of OHT at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · OHT

25in 2025

2010: 12012: 12013: 22014: 42015: 22016: 32017: 62018: 82019: 72020: 12021: 122022: 252023: 322024: 262025: 252026 (partial year): 11
2007high 32 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OHT

87in 2025

2014: 166 days median2016: 81 days median2017: 87 days median2018: 89 days median2019: 64 days median2021: 89 days median2022: 70 days median2023: 83 days median2024: 62 days median2025: 87 days median2026 (partial year): 84 days median
2007high 166 (2014) · low 62 (2024)2026

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

Recalls per year · OHT

No recall names OHT since 2007.

Adverse event reports per year · OHT

6in 2025

2015: 12016: 22019: 22020: 32021: 12022: 22023: 62025: 6
2007high 6 (2023) · low 0 (2007)2025

MAUDE reports naming product code OHT, 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
20070—00
20080—00
20090—00
20101—00
20110—00
20121—00
20132—00
2014416600
20152—01
201638102
201768700
201888900
201976402
20201—03
2021128901
2022257002
2023328306
2024266200
2025258706
202611840—
FIG. 1 — OHT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OHT? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 878.4810.