DORSAVI LTD

FDA Device Registration & Listing · Oakleigh South Victoria, AU · Registration 3010872373

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010872373
FEI Number
3010872373
Entity Name
DORSAVI LTD
City/State/Country
Oakleigh South Victoria, AU
Establishment Address
3 / 11-13 Milgate Street, Oakleigh South Victoria 3167, AU
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
dorsaVi Ltd (Owner Number: 10046462)
Owner / Operator Contact Address
3 / 11-13 Milgate Street, Oakleigh South, AU-VIC 3167, AU
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Professional Suite ViMove+ Movement Suite Professional Suite Movement Suite ViMove+

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2014-07-15
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2014-07-15
IKN Electromyograph, Diagnostic Physical Medicine Class 2 890.1375 2014-07-15
HCC Device, Biofeedback Neurology Class 2 882.5050 2017-07-15
IKN Electromyograph, Diagnostic Physical Medicine Class 2 890.1375 2017-07-15
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2017-07-15

Official Correspondent

Dan Ronchi

US Agent Details

Mary (Maka) Lange (nee Stewart) Business: dorsaVi USA Inc. Email: regulatory@dorsavi.com Phone: (847) 6912928

Related Public Records

Same Entity

dorsaVi Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010872373. Last updated year: 2026. Please use registration number 3010872373 when referencing this establishment in official correspondence.
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