510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K213830Substantially Equivalent

Home use hair removal device, model: Precise Touch Pro

Iluminage Beauty Co., Limited, Wan Chai, HK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213830 is the FDA 510(k) clearance record for Home use hair removal device, model: Precise Touch Pro, a class II device, cleared for Iluminage Beauty Co., Limited on under FDA product code OHT (Light Based Over-The-Counter Hair Removal). FDA's definition for product code OHT reads: "Over-the-counter device uses thermal energy to kill hair follicles for hair removal". FDA records list one 510(k) clearance for Iluminage Beauty Co., Limited. As of , FDA records show no recalls naming K213830.

Clearance record

Decision date
Received
(55 days to decision)
Product code
OHT Light Based Over-The-Counter Hair Removal
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Iluminage Beauty Co., Limited Level 54, Hopewell Centre, 183 Queen'S Rd. E., Wan Chai, HK
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OHT

Trailing 12 months
15 clearances under product code OHT in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code OHT, trailing twelve months
MonthClearances
November 20253
December 20252
January 20260
February 20261
March 20261
April 20261
May 20263
June 20260
July 20260
August 20261
September 20263
October 20260