ZIIP Beauty

FDA UDI

Class II (US FDA UDI)

by Ziip, Llc

Identity

Trade Name: ZIIP Beauty FDA UDI
Generic Name: Facial muscle cosmesis electrical stimulator FDA UDI
Device Name: ZIIP HALO DEVICE FDA UDI
Model / Reference: HALO FDA UDI
Description: ZIIP HALO DEVICE FDA UDI

Identifiers

Primary DI / UDI-DI: 00851367006149 FDA UDI
510(k) Number: K212342 FDA UDI
FDA Product Code: NFO FDA UDI
GMDN Term: Facial muscle cosmesis electrical stimulator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.5890 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Facial muscle cosmesis electrical stimulator

ZIIP Beauty by Ziip, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K212342 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ziip, Llc

Sources (1)

FDA UDI bdbdb5b7-0e8a-4e3b-bcf5-bf966d3a0b9a 36 fields · synced May 30, 2026