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Rite Aid SI30

by Rite Aid Corporation

Rite Aid SI30 is a home-use facial steamer (FDA Class I; FDA product code KFZ, Humidifier, Non-Direct Patient Interface (Home-Use)) made by Rite Aid Corporation, listed in FDA GUDID since 31 May 2022 (UDI-DI 00011822820356), 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 Number00011822820356 UDI-DI Date31 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  • Withdrawn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
Rite Aid
Generic name
Home-use facial steamer
Model / reference
SI30
Primary DI / UDI-DI
00011822820356
FDA product code
KFZ
GMDN term
Home-use facial steamer
Device class
Class I
Regulation number
868.5460
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KFZ (Humidifier, Non-Direct Patient Interface (Home-Use)).

Other devices from Rite Aid Corporation

See all devices from Rite Aid Corporation →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)