VQ ORTHOCARE

FDA Device Registration & Listing · VISTA, CA, US · Registration 2031823

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
2031823
FEI Number
3002757749
Entity Name
VQ ORTHOCARE
City/State/Country
VISTA, CA, US
Establishment Address
1390 Decision St Ste A, VISTA, CA 92081, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
VISION QUEST INDUSTRIES, INC. (Owner Number: 9022498)
Owner / Operator Contact Address
1390 Decision St, Suite A, --, Vista, CA 92081, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Triple Play EZ-Fit VT Compression Foot Sleeve - TP-3434VQ Triple Play EZ-Fit VT Leg Sleeve Extension Panels - TP-3636-EXTVQ Compression Calf Sleeve - TP-3333VQ Triple Play Pro Facility Compression Pump - TPVT-01PVQ Triple Play EZ-Fit VT Compression Leg Sleeve - TP-3636VQ Triple Play EZ-Fit VT Calf Wrap Extension Panels - TP-3333-EXTVQ VQ Knee Suspension Sleeve KN208 LSO ASCENT APL LG/XL VQ LSO 627 LSO ASCENT AP SM/MD ASCENT TLSO LSO ASCENT APL SM/MD LSO ASCENT AP LG/XL LSO ASCENT AP+ SM/MD LSO ASCENT AP+ LG/XL VQ LSO 637 VQ LSO 631 AVID CT2 BioniCare Knee ECLIPSE EXT CERVICAL COLLAR ECLIPSE CERVICAL COLLAR AVID IF2 Interferential Stimulator Triple Play Compression Pump - TPVT-01AVQ VQ Functional Arm Brace Catalyst Propel OA TRUlign OA Glyde OA OActive 2 OActive Catalyst Elite Catalyst Propel ROM OActive Align Catalyst Propel BioniCare Knee BioniCare Hand VQ-Flow Compression System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2019-11-04
IPY Orthosis, Lumbo-Sacral Physical Medicine Class 1 890.3490 2005-04-21
LIH Interferential Current Therapy Neurology Class 2 882.5890 2022-03-19
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2022-03-19
NYN Stimulator, Electrical, Transcutaneous, For Arthritis Neurology Class 2 882.5890 2011-12-21
IQF Orthosis, Cervical-Thoracic, Rigid Physical Medicine Class 1 890.3490 2015-03-16
LIH Interferential Current Therapy Neurology Class 2 882.5890 2019-11-04
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2019-11-04
IOY Support, Arm Physical Medicine Class 1 890.3475 2005-04-04
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2001-11-28
NYN Stimulator, Electrical, Transcutaneous, For Arthritis Neurology Class 2 882.5890 2011-12-21
NYN Stimulator, Electrical, Transcutaneous, For Arthritis Neurology Class 2 882.5890 2013-01-16
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2022-06-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VISION QUEST INDUSTRIES, INC.
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
K170216 Tactile Systems Technology, Inc. (Dba Tactile Medical) Flexitouch System 2017-05-26
K100306 Covidien KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES 2010-05-04
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2031823. Last updated year: 2026. Please use registration number 2031823 when referencing this establishment in official correspondence.
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