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IPL Home Use Hair Removal Device

FDA UDI

Class II (US FDA UDI)

by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

Identity

Trade Name
IPL Home Use Hair Removal Device FDA UDI
Generic Name
Home-use intense pulsed light hair removal unit FDA UDI
Device Name
The Device is an over-the-counter device intended for removal of unwanted body and/or facial hair. FDA UDI
Model / Reference
D-T1002 FDA UDI
Description
The Device is an over-the-counter device intended for removal of unwanted body and/or facial hair. FDA UDI

Identifiers

Primary DI / UDI-DI
06974879930024 FDA UDI
510(k) Number
K211922 FDA UDI
FDA Product Code
OHT FDA UDI
GMDN Term
Home-use intense pulsed light hair removal unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Home-use intense pulsed light hair removal unit

IPL Home Use Hair Removal Device by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Home-use intense pulsed light hair removal unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24a76ab5-b7b3-4276-b757-d75308b8330c 34 fields · synced May 30, 2026