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iQ Elevation 1

by First Source Inc.

iQ Elevation 1 (100DRWBS) is a radiological general body-part positioner (FDA Class I; FDA product code KXH, Cradle, Patient, Radiologic) made by First Source Inc., listed in FDA GUDID since 12 Jun 2023 (UDI-DI G221100DRWBS0), 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 NumberG221100DRWBS0 UDI-DI Date12 Jun 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
iQ Elevation
Generic name
Radiological general body-part positioner
Model / Ref / Catalog
1, 100DRWBS
Primary DI / UDI-DI
G221100DRWBS0
FDA product code
KXH
GMDN term
Radiological general body-part positioner
Device class
Class I
Regulation number
892.1830
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radiological general body-part positioner

Similar devices

Other devices filed under FDA product code KXH (Cradle, Patient, Radiologic).

Other devices from First Source Inc.

  • iQ Flex Pro

    Class II

  • iQ Flex Edge

    Class I

  • iQ View V5

    Class II

  • iQ Flex MD Open recall

    Class II

See all devices from First Source Inc. →

Properties

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