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bt-sculpt MF-77

by Micro Current Technology, Inc.

bt-sculpt MF-77 is a medical device (FDA Class II; FDA product code NFO, Stimulator, Transcutaneous Electrical, Aesthetic Purposes) made by Micro Current Technology, Inc., listed in FDA GUDID since 28 Feb 2024 (UDI-DI 00817076014219), 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 Number00817076014219 UDI-DI Date28 Feb 2024ListedStatusListed 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  • Withdrawn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
bt-sculpt
Generic name
Analgesic transcutaneous electrical nerve stimulation system
Model / reference
MF-77
Primary DI / UDI-DI
00817076014219
FDA product code
NFO
GMDN term
Analgesic transcutaneous electrical nerve stimulation system
Device class
Class II
Regulation number
882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Category: Analgesic transcutaneous electrical nerve stimulation system

Similar devices

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

Other devices from Micro Current Technology, Inc.

See all devices from Micro Current Technology, Inc. →

Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)