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Nuon HD-44

by Shenzhen Nuon Medical Equipment 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 Number06977168990013 UDI-DI Date21 Apr 2026ListedStatusListed 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  • Withdrawn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
Nuon
Generic Name
Hand-held deep-tissue electromagnetic stimulator
Model / Reference
HD-44
Primary DI / UDI-DI
06977168990013
510(k) Number
FDA Product Code
NFO
GMDN Term
Hand-held deep-tissue electromagnetic stimulator
Device Class
Class II
Regulation Number
882.5890
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Nuon Medical Equipment Co., Ltd.

See all devices from Shenzhen Nuon Medical Equipment 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