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JOVS Graphene Hair Removal Device

FDA UDI

Class II (US FDA UDI)

by Shenzhen Qianyu Technology Co., Ltd.

Identity

Trade Name
JOVS Graphene Hair Removal Device FDA UDI
Generic Name
Intense pulsed light skin surface treatment system FDA UDI
Model / Reference
JOC-910-Emerald FDA UDI

Identifiers

Primary DI / UDI-DI
06973698659208 FDA UDI
510(k) Number
K214113 FDA UDI
FDA Product Code
OHT FDA UDI
GMDN Term
Intense pulsed light skin surface treatment system 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intense pulsed light skin surface treatment system

JOVS Graphene Hair Removal Device by Shenzhen Qianyu Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intense pulsed light skin surface treatment system.

Cleared under the same submission

K214113 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Qianyu Technology Co., Ltd.

Sources (1)

  • FDA UDI f6efd8a8-9226-4fbb-811c-e6a3ac6643d8 33 fields · synced Jun 8, 2026