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FLIP Lube

FDA UDI

Class II (US FDA UDI)

by Lubrinovation, Inc.

Identity

Trade Name
FLIP Lube FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
4 oz. bottle of FLIP Lube personal lubricant FDA UDI
Model / Reference
1 FDA UDI
Description
4 oz. bottle of FLIP Lube personal lubricant FDA UDI

Identifiers

Primary DI / UDI-DI
00853517007013 FDA UDI
510(k) Number
K171516 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sexual lubricant

FLIP Lube by Lubrinovation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sexual lubricant.

Cleared under the same submission

K171516 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lubrinovation, Inc.

Sources (1)

  • FDA UDI 1baa855a-d99d-4c89-9348-921b3c630959 36 fields · synced May 30, 2026