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Ultroting XTS-B06-L

by Shenzhen Magnet Technology 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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06979053570034 UDI-DI Date21 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ultroting
Generic Name
Air-conduction hearing aid, in-the-ear
Model / Reference
XTS-B06-L
Primary DI / UDI-DI
06979053570034
FDA Product Code
QUF
GMDN Term
Air-conduction hearing aid, in-the-ear
Device Class
Class I
Regulation Number
874.3300
GUDID distribution status
In Commercial Distribution

Other devices from Shenzen Magnet Technology Co., Ltd

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • 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
  • Expiration Date: No