← Back to catalogue

BlowYo

FDA UDI

Class II (US FDA UDI)

by Westridge Laboratories Incorporated

Identity

Trade Name
BlowYo FDA UDI
Generic Name
Sexual lubricant FDA UDI
Model / Reference
BlowYo Water Based 3.4 fl oz FDA UDI

Identifiers

Primary DI / UDI-DI
05060020002663 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

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

Dimensions & Sizes

Size
Total Volume — 3.4 Fluid Ounce FDA UDI

Category: Sexual lubricant

BlowYo 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2a43c4fd-ee84-4024-9b8c-1352305e024c 34 fields · synced Jun 6, 2026