Skip to content

hipEOS 3.2

by Eos Imaging

hipEOS 3.2 is a Class II device made by Eos Imaging, listed in FDA GUDID since 10 Jul 2023 (UDI-DI 03663999000177), not in commercial distribution (GUDID) as of 12 Nov 2026.

Listed FDA GUDID listing, not in commercial distribution

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03663999000177 UDI-DI Date10 Jul 2023ListedStatusListed GUDID: not 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  • Withdrawn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
hipEOS
Generic name
Orthopaedic/craniofacial implantation planning software
Model / reference
3.2
Primary DI / UDI-DI
03663999000177
FDA product code
LLZ
GMDN term
Orthopaedic/craniofacial implantation planning software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

Other devices from Eos Imaging

  • spineEOS 6.x

    Class II

  • AutoDensity 1.3

    Class II

  • VEA Align 4.x

    Class II

  • EOS System

    Class II

See all devices from Eos Imaging →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)