Cleared Traditional

Home use hair removal device, model: Precise Touch Pro (K213830) - FDA 510(k) Clearance

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K213830 · Iluminage Beauty Co., Limited · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2022
Decision
55d
Days
Class 2
Risk

K213830 is an FDA 510(k) clearance for the Home use hair removal device, model: Precise Touch Pro. Classified as Light Based Over-the-counter Hair Removal (product code OHT), Class II - Special Controls.

Submitted by Iluminage Beauty Co., Limited (Wan Chai, HK). The FDA issued a Cleared decision on February 1, 2022 after a review of 55 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4810 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Iluminage Beauty Co., Limited devices

Submission Details

510(k) Number K213830 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 2021
Decision Date February 01, 2022
Days to Decision 55 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 115d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code OHT Light Based Over-the-counter Hair Removal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4810
Definition Over-the-counter Device Uses Thermal Energy To Kill Hair Follicles For Hair Removal.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Consultant

Feiying Drug & Medical Consulting Technical Service Group
Rain Yip

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - OHT Light Based Over-the-counter Hair Removal

All 141
Devices cleared under the same product code (OHT) and FDA review panel - the closest regulatory comparables to K213830.
IPL Hair Removal Device, model(s): S1-A, S2-A, S1, S2, S3, S4
K220222 · Shenzhen Yuwei Electronic Technology Co., Ltd. · Apr 2022
Intense Pulsed Light (IPL) System
K212881 · Shenzhen Fansizhe Science And Technology Co., Ltd. · Apr 2022
Hand-held IPL device(JOVS Graphene Hair Removal Device)
K214113 · Shenzhen Qianyu Technology Co., Ltd. · Mar 2022
SmoothSkin Pure Mini
K213692 · Cyden Limited · Jan 2022
IPL Hair Removal
K212318 · Dongguan Define Beauty Electronic Technology Co., Ltd. · Jan 2022
IPL Home Use Hair Removal Device
K211185 · Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. · Dec 2021