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YEAHONE IPL Home Use Hair Removal Device(SJ15)

by Shenzhen shuge medical beauty devices co., ltd.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975969046014 UDI-DI Date6 Aug 2024ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Yeahone
Generic Name
Home-use intense pulsed light hair removal unit
Model / Reference
IPL Home Use Hair Removal Device(SJ15)
Primary DI / UDI-DI
06975969046014
510(k) Number
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
Not in Commercial Distribution

Other devices from Shenzhen shuge medical beauty devices co., ltd.

Properties

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

Other properties (9)

  • 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