V&Q

FDA UDI

Class II (US FDA UDI)

by V & Q Manufacturing Corporation

Identity

Trade Name: V&Q FDA UDI
Generic Name: Surgical/medical face mask, single-use FDA UDI
Device Name: Non Woven Face Mask is intended for single use by operating room personnel and other general healthcare workers to protect both patients and healthcare workers against transfer of microorganisms, blood and body fluids, and particulate materials. FDA UDI
Model / Reference: VQN0185B FDA UDI
Description: Non Woven Face Mask is intended for single use by operating room personnel and other general healthcare workers to protect both patients and healthcare workers against transfer of microorganisms, blood and body fluids, and particulate materials. FDA UDI

Identifiers

Primary DI / UDI-DI: 06970272170036 FDA UDI
510(k) Number: K173062 FDA UDI
FDA Product Code: FXX FDA UDI
GMDN Term: Surgical/medical face mask, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/medical face mask, single-use

V&Q by V & Q Manufacturing Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, single-use.

ProGear — Prestige Ameritech · Class II
Precept® — Precept Medical Products, Inc. · Class II
hcs — DYAD MEDICAL SOURCING, LLC · Class I
Precept® — Precept Medical Products, Inc. · Class II
AOSHANG — Tianjin Aoshang Outdoor Equipment Co., Ltd. · Class II
Precept® — Precept Medical Products, Inc. · Class II
Precept® — Precept Medical Products, Inc. · Class II
Surgical Face Mask — Foshan Nanhai Plus Medical Co., Ltd · Class II

Cleared under the same submission

K173062 also covers:

HYGITECH — HYGITECH
HYGITECH — HYGITECH
HYGITECH — HYGITECH
HYGITECH — HYGITECH
HYGITECH — HYGITECH
HYGITECH — HYGITECH
HYGITECH — HYGITECH
PureDefense Surgical Mask — MEDIVISION, INC.
PureDefense Surgical Mask — MEDIVISION, INC.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: V & Q Manufacturing Corporation

Sources (1)

FDA UDI 5249199f-174b-45fb-afdf-985c981f94b0 35 fields · synced May 30, 2026