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

Facial & Body Beauty Device (model: INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)

K Number: K253833 · Decision Jan 30, 2026
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
152
Applicant Total
4
Review Days
60

Basic Information

Device Name
Facial & Body Beauty Device (model: INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)
K Number
K253833
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
Shenzhen Jianchao Intelligent Technology Co., Ltd.
Date Received
December 1, 2025
Decision Date
January 30, 2026
Product Code
OHS
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
OHS Light Based Over The Counter Wrinkle Reduction

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OHS), ordered by most recent decision date.

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Other Clearances by Shenzhen Jianchao Intelligent Technology Co., Ltd.

K Number Device Name
K252553 Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)
K242710 Hair Removal Device (R3C16-P, R3C16-W, R3C16-G, R3C16-P Pro, R3C16-W Pro, R3C16-G Pro, R3505-W, R3505-B, R3505-W Pro, R3505-B Pro)
K232575 Hair Removal Device, Model(s): R2815-G Pro, R2815-G