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Summit S225

by Summit Industries, LLC

Summit S225 is a Class I device made by Summit Industries, LLC, listed in FDA GUDID since 7 Nov 2016 (UDI-DI B307S2250), 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 NumberB307S2250 UDI-DI Date7 Nov 2016ListedStatusListed 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  • Withdrawn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
Summit
Generic name
X-ray system tube support, floor standing
Model / Ref / Catalog
S225
Primary DI / UDI-DI
B307S2250
FDA product code
IYB
GMDN term
X-ray system tube support, floor standing
Device class
Class I
Regulation number
892.1770
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IYB (Tube Mount, X-Ray, Diagnostic).

Other devices from Summit Industries, LLC

See all devices from Summit Industries, LLC →

Properties

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