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9406

by Domico Med-Device, LLC

9406 is a Class II device made by Domico Med-Device, LLC, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10810050242728), 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 Number10810050242728 UDI-DI Date24 Sep 2020ListedStatusListed 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  • Withdrawn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

Generic name
Multifunction body cushion
Model / reference
9406
Primary DI / UDI-DI
10810050242728
FDA product code
KXJ, CCX
GMDN term
Multifunction body cushion
Device class
Class II
Regulation number
892.1980, 868.6820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multifunction body cushionRadiological arm/leg positioner

Other devices from Domico Med-Device, LLC

See all devices from Domico Med-Device, LLC →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)