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Flex Gar Sock SOCK0001

by Emsi

Flex Gar Sock SOCK0001 is a Class II device made by Emsi, listed in FDA GUDID since 5 Sep 2016 (UDI-DI 00858688006230), 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 Number00858688006230 UDI-DI Date5 Sep 2016ListedStatusListed 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  • Withdrawn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
Flex Gar Sock
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / reference
SOCK0001
Primary DI / UDI-DI
00858688006230
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

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Properties

  • Lot / batch number
Other properties (14, all answered No)