IPL Hair Removal Device JP1

by Shenzhen Jvk Medical Instruments Co., Ltd

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06977449410018 UDI-DI	Date12 Sep 2025Listed	StatusListed GUDID: in commercial distribution

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Withdrawn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: JP1

Primary DI / UDI-DI: 06977449410018
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 Shenzhen Jvk Medical Instruments Co., Ltd

Properties

Over-the-Counter
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No