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Vq Orthocare

FDA UDI

Class II (US FDA UDI)

by Vision Quest Industries Incorporated

Identity

Trade Name
VQ ORTHOCARE FDA UDI
Generic Name
Arthritis transcutaneous electrical joint stimulation system FDA UDI
Device Name
BIONICARE KNEE SYSTEM LEFT S/M FDA UDI
Model / Reference
55-95003-201 FDA UDI
Description
BIONICARE KNEE SYSTEM LEFT S/M FDA UDI

Identifiers

Primary DI / UDI-DI
00817717020197 FDA UDI
510(k) Number
K030332 FDA UDI
FDA Product Code
NYN FDA UDI
GMDN Term
Arthritis transcutaneous electrical joint stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arthritis transcutaneous electrical joint stimulation system

Vq Orthocare by Vision Quest Industries Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthritis transcutaneous electrical joint stimulation system.

Cleared under the same submission

K030332 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vision Quest Industries Incorporated

Sources (1)

  • FDA UDI a3972e11-c002-444c-9e73-8fe3fdcaf295 34 fields · synced May 30, 2026