FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C)

K Number: K253304 · Decision Nov 25, 2025
Classifications
1
FEI Numbers
90
Registration Numbers
91
Same Product Code
161
Applicant Total
2
Review Days
57

Basic Information

Device Name
IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C)
K Number
K253304
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dongguan Lide Electric Appliance Co., Ltd.
Date Received
September 29, 2025
Decision Date
November 25, 2025
Product Code
OHT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OHT Light Based Over-The-Counter Hair Removal

Similar 510(k) Clearances

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Other Clearances by Dongguan Lide Electric Appliance Co., Ltd.

K Number Device Name
K232056 IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002