← Back to catalogue

KY Liquid Lubricant

FDA UDI

Class II (US FDA UDI)

by RB Health (us) LLC

Identity

Trade Name
KY Liquid Lubricant FDA UDI
Generic Name
Vaginal lubricant FDA UDI
Device Name
Personal Lubricant FDA UDI
Model / Reference
Personal Lubricant FDA UDI
Description
Personal Lubricant FDA UDI

Identifiers

Primary DI / UDI-DI
88067981087909 FDA UDI
510(k) Number
K193032 FDA UDI
K955648 FDA UDI
FDA Product Code
HIS FDA UDI
NUC FDA UDI
GMDN Term
Vaginal lubricant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5300 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

KY Liquid Lubricant by RB Health (us) LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K193032 also covers:

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

Manufacturer
RB Health (us) LLC

Sources (1)

  • FDA UDI e1ddb9f3-bb16-4b43-8504-5118dc2c96b2 37 fields · synced Jun 1, 2026