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Jmoon M30U Sg

by Shenzhen Ulike Smart Electronics Co., Ltd.

Jmoon M30U Sg is a Class II device made by Shenzhen Ulike Smart Electronics Co., Ltd., listed in FDA GUDID since 7 Jun 2025 (UDI-DI 06974667825037), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974667825037 UDI-DI Date7 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Jmoon
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / reference
M30U SG
Primary DI / UDI-DI
06974667825037
FDA product code
NFO, OHS
GMDN term
Physical therapy transcutaneous neuromuscular electrical stimulation system
Device class
Class II
Regulation number
882.5890, 878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Physical therapy transcutaneous neuromuscular electrical stimulation systemCosmetic red-light phototherapy system, home-use

Similar devices

Other devices filed under FDA product code NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes).

Other devices from Shenzhen Ulike Smart Electronics Co., Ltd

See all devices from Shenzhen Ulike Smart Electronics Co., Ltd →

Properties

  • Over-the-counter
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)