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Lovehoney Cherry

FDA UDI

Class II (US FDA UDI)

by Westridge Laboratories Incorporated

Identity

Trade Name
Lovehoney Cherry FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
Lovehoney Cherry water based lubricant. FDA UDI
Model / Reference
Lovehoney Cherry 3.4oz FDA UDI
Description
Lovehoney Cherry water based lubricant. FDA UDI

Identifiers

Catalog Number
IDD11350 FDA UDI
Primary DI / UDI-DI
05060493009862 FDA UDI
510(k) Number
K051295 FDA UDI
FDA Product Code
NUC FDA UDI
GMDN Term
Sexual lubricant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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: Sexual lubricant

Lovehoney Cherry by Westridge Laboratories Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sexual lubricant.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e83ec92-e432-4271-9a32-9e2b4c5025f7 35 fields · synced May 30, 2026