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Skyn

FDA UDI

Class II (US FDA UDI)

by Suretex Limited - Branch

Identity

Trade Name
SKYN FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
SKYN NATURALLY ENDLESS 8.5fl oz (250ml) FDA UDI
Model / Reference
0115 FDA UDI
Description
SKYN NATURALLY ENDLESS 8.5fl oz (250ml) FDA UDI

Identifiers

Primary DI / UDI-DI
00070907001158 FDA UDI
510(k) Number
K221243 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sexual lubricant

Skyn by Suretex Limited - Branch — 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 dc6a9d18-8852-4c2a-a45c-f745bab2b0b0 35 fields · synced May 30, 2026