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Sword Bloom 7

by Sword Health, S.A.

Sword Bloom 7 is a Class II device made by Sword Health, S.A., listed in FDA GUDID since 25 Jul 2024 (UDI-DI 05065013876023), 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 Number05065013876023 UDI-DI Date25 Jul 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  • Withdrawn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
Sword Bloom
Generic name
Pelvic floor muscle exerciser
Model / reference
7
Primary DI / UDI-DI
05065013876023
FDA product code
KXQ
GMDN term
Pelvic floor muscle exerciser
Device class
Class II
Regulation number
884.5960
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pelvic floor muscle exerciser

Similar devices

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

Other devices from Sword Health, S.A.

See all devices from Sword Health, S.A. →

Properties

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