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Fynelook EE0101

by Shenzhen Dachi Communication Co., Ltd.

Listed FDA GUDID listing, no authorization on record

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 Number06979082450000 UDI-DI Date2 Dec 2025ListedStatusListed GUDID: 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  • Withdrawn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
Fynelook
Generic Name
Transcutaneous electrical stimulation probe
Model / Reference
EE0101
Primary DI / UDI-DI
06979082450000
510(k) Number
FDA Product Code
NFO
GMDN Term
Transcutaneous electrical stimulation probe
Device Class
Class II
Regulation Number
882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K244004)

Other devices from Shenzhen Dachi Communication Co., Ltd.

Properties

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

Other properties (11)

  • 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
  • Expiration Date: No