IPL Hair Removal device Skin Expert Pro IPL008S

by Zhongshan Qizhe Technology Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06973426820818 UDI-DI	Date25 Oct 2023Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: IPL Hair Removal device
Generic Name: Home-use intense pulsed light hair removal unit
Model / Reference: Skin Expert Pro IPL008S

Primary DI / UDI-DI: 06973426820818
510(k) Number: K231215
FDA Product Code: OHT
GMDN Term: Home-use intense pulsed light hair removal unit

Device Class: Class II
Regulation Number: 878.4810
GUDID distribution status: In Commercial Distribution

Other devices from Zhongshan Qizhe Technology Co., Ltd.

Properties

Serial Number
Manufacturing Date

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No