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VMA Motion Normalizer 3

by Ortho Kinematics, Inc.

VMA Motion Normalizer 3 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Ortho Kinematics, Inc., listed in FDA GUDID since 31 Jan 2018 (UDI-DI 00868579000247), 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 Number00868579000247 UDI-DI Date31 Jan 2018ListedStatusListed 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  • Withdrawn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
VMA Motion Normalizer
Generic name
Diagnostic x-ray digital imaging system workstation
Model / reference
3
Primary DI / UDI-DI
00868579000247
FDA product code
LLZ
GMDN term
Diagnostic x-ray digital imaging system workstation
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Diagnostic x-ray digital imaging system workstation

Similar devices

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

Other devices from Ortho Kinematics, Inc.

See all devices from Ortho Kinematics, Inc. →

Properties

  • Serial number
Other properties (14, all answered No)