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Fizimed Emy V1

by Fizimed

Fizimed Emy V1 is a perineometer (FDA Class II; FDA product code KXQ, Vibrator For Therapeutic Use, Genital) made by Fizimed, listed in FDA GUDID since 16 May 2022 (UDI-DI 03770011873005), 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 Number03770011873005 UDI-DI Date16 May 2022ListedStatusListed 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  • Withdrawn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
Fizimed
Generic name
Perineometer
Model / reference
Emy V1
Primary DI / UDI-DI
03770011873005
FDA product code
KXQ
GMDN term
Perineometer
Device class
Class II
Regulation number
884.5960
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perineometer

Similar devices

Other devices filed under FDA product code KXQ (Vibrator For Therapeutic Use, Genital).

Other devices from Fizimed

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)