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Transcutaneous Electrical Nerve Stimulators KTR-2402

by Shenzhen Kentro Medical Electronics Co., Ltd 2 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06924607703550 UDI-DI Date31 Jul 2026ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Transcutaneous Electrical Nerve Stimulators
Generic Name
Analgesic transcutaneous electrical nerve stimulation system
Model / Reference
KTR-2402
Primary DI / UDI-DI
06924607703550
510(k) Number
FDA Product Code
NUH, NYG
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system
Device Class
Class II
Regulation Number
882.5890, 872.4565
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K232517)

Other devices from Shenzhen Kentro Medical Electronics Co., Ltd

See all devices from Shenzhen Kentro Medical Electronics Co., Ltd →

Properties

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