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Restore Moisturizing Vaginal Gel

FDA UDI

Class I (US FDA UDI)

by Good Clean Love, Inc.

Identity

Trade Name
Restore Moisturizing Vaginal Gel FDA UDI
Generic Name
General-body orifice lubricant, non-sterile FDA UDI
Device Name
Restore is a patient lubricant intended for medical purposes that is used to lubricate a body orifice to facilitate entry of a diagnostic or therapeutic device. FDA UDI
Model / Reference
2 oz FDA UDI
Description
Restore is a patient lubricant intended for medical purposes that is used to lubricate a body orifice to facilitate entry of a diagnostic or therapeutic device. FDA UDI

Identifiers

Catalog Number
900300 FDA UDI
Primary DI / UDI-DI
00850014621476 FDA UDI
FDA Product Code
KMJ FDA UDI
GMDN Term
General-body orifice lubricant, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6375 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-body orifice lubricant, non-sterile

Restore Moisturizing Vaginal Gel by Good Clean Love, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-body orifice lubricant, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Good Clean Love, Inc.

Sources (1)

  • FDA UDI 14833997-7a18-4fc9-8c56-edfc23f69827 35 fields · synced May 30, 2026