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iQ Flex Pro

by First Source Inc.

iQ Flex Pro (500MC009) is a diagnostic x-ray system generator (FDA Class II; FDA product code IZL, System, X-Ray, Mobile) made by First Source Inc., listed in FDA GUDID since 25 Aug 2026 (UDI-DI G221500MC009H0), 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 NumberG221500MC009H0 UDI-DI Date25 Aug 2026ListedStatusListed 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  • Withdrawn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 Flex
Generic name
Diagnostic x-ray system generator, portable
Model / Ref / Catalog
Pro, 500MC009
Primary DI / UDI-DI
G221500MC009H0
FDA product code
IZL
GMDN term
Diagnostic x-ray system generator, portable
Device class
Class II
Regulation number
892.1720
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IZL (System, X-Ray, Mobile).

Other devices from First Source Inc.

  • iQ Flex Edge

    Class I

  • iQ View V5

    Class II

  • iQ Flex MD Open recall

    Class II

  • iQ Elevation 1

    Class I

See all devices from First Source Inc. →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)