Skip to content

interWORKS Version 8.9.0.21783

by Avreo, Inc.

interWORKS Version 8.9.0.21783 is a Class I device made by Avreo, Inc., listed in FDA GUDID since 3 Aug 2026 (UDI-DI 00850054590183), 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 Number00850054590183 UDI-DI Date3 Aug 2026ListedStatusListed 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  • Withdrawn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
interWORKS
Generic name
Radiology information system
Model / reference
Version 8.9.0.21783
Primary DI / UDI-DI
00850054590183
FDA product code
LMD
GMDN term
Radiology information system
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

Other devices from Avreo, Inc.

See all devices from Avreo, Inc. →

Properties

  • Prescription use
Other properties (14, all answered No)