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Slendertone Evolve Abs 735

by Bio-Medical Research, Ltd.

Slendertone Evolve Abs (735-5000) is a transcutaneous electrical stimulation electrode (FDA Class II; FDA product code NGX, Stimulator, Muscle, Powered, For Muscle Conditioning) made by Bio-Medical Research, Ltd., listed in FDA GUDID since 26 Mar 2021 (UDI-DI 15099058735004), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number15099058735004 UDI-DI Date26 Mar 2021ListedStatusListed 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  • Withdrawn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
Slendertone Evolve Abs
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / Ref / Catalog
735, 735-5000
Primary DI / UDI-DI
15099058735004
FDA product code
NGX
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
890.5850
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NGX (Stimulator, Muscle, Powered, For Muscle Conditioning).

Other devices from Bio-Medical Research, Ltd.

See all devices from Bio-Medical Research, Ltd. →

Properties

  • Over-the-counter
  • Convenience kit
  • Serial number
  • Expiration date
Other properties (11, all answered No)