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FusionXC FM-XC358006

by Moxi Enterprises, LLC

FusionXC FM-XC358006 is an orthopaedic bed mattress (FDA Class I; FDA product code IKY, Mattress, Flotation Therapy, Non-Powered) made by Moxi Enterprises, LLC, listed in FDA GUDID since 11 Aug 2016 (UDI-DI 00817365020341), 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 Number00817365020341 UDI-DI Date11 Aug 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  • Withdrawn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
FusionXC
Generic name
Orthopaedic bed mattress
Model / Ref / Catalog
FM-XC358006
Primary DI / UDI-DI
00817365020341
FDA product code
IKY
GMDN term
Orthopaedic bed mattress
Device class
Class I
Regulation number
880.5150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bed mattress

Similar devices

Other devices filed under FDA product code IKY (Mattress, Flotation Therapy, Non-Powered).

Other devices from Moxi Enterprises, LLC

See all devices from Moxi Enterprises, LLC →

Properties

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