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Vq Orthocare

FDA UDI

Class I (US FDA UDI)

by Vision Quest Industries Incorporated

Identity

Trade Name
VQ ORTHOCARE FDA UDI
Generic Name
Knee support orthosis FDA UDI
Device Name
CATALYST PROPEL OA DBL Q HINGE CUST LFT FDA UDI
Model / Reference
07-42003-001 FDA UDI
Description
CATALYST PROPEL OA DBL Q HINGE CUST LFT FDA UDI

Identifiers

Primary DI / UDI-DI
00817717020739 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Knee support orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee support orthosis

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

Similar devices

Also classified as Knee support orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5d3a8de-de2d-4f9c-badb-f8a2f510e6f3 33 fields · synced Jun 8, 2026