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Nu Skin Facial Spa Package

FDA UDI

Class II (US FDA UDI)

by Nse Products, Inc.

Identity

Trade Name
Nu Skin Facial Spa Package FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Model / Reference
1001352 FDA UDI

Identifiers

Primary DI / UDI-DI
00860196000327 FDA UDI
510(k) Number
K022006 FDA UDI
K122711 FDA UDI
FDA Product Code
NFO FDA UDI
GYB FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
882.1275 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

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation systemSkin topical coupling gelTranscutaneous electrical stimulation probe

Nu Skin Facial Spa Package by Nse Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation probe.

Cleared under the same submission

K022006 also covers:

K122711 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nse Products, Inc.

Sources (1)

  • FDA UDI b7d7f445-3a2f-4116-bf6b-ba50efff86ef 34 fields · synced Jun 8, 2026