Revian Inc. Replacement Kit USB-C Power Cable

FDA UDI

Class II (US FDA UDI)

by Revian, Inc.

Identity

Trade Name: Revian Inc. Replacement Kit USB-C Power Cable FDA UDI
Generic Name: Hair growth laser device FDA UDI
Device Name: The Revian USB-C Power Cable Replacement Kit is a kit that may be shipped to users of the REVIAN Red device (Catalog 10001) or REVIAN Lyte device (Catalog 10011) who have lost or misplaced the power cable originally supplied with the hair regrowth device. FDA UDI
Model / Reference: 10000-12723 FDA UDI
Description: The Revian USB-C Power Cable Replacement Kit is a kit that may be shipped to users of the REVIAN Red device (Catalog 10001) or REVIAN Lyte device (Catalog 10011) who have lost or misplaced the power cable originally supplied with the hair regrowth device. FDA UDI

Identifiers

Catalog Number: 12723 FDA UDI
Primary DI / UDI-DI: 00850003374147 FDA UDI
510(k) Number: K173729 FDA UDI
FDA Product Code: OAP FDA UDI
GMDN Term: Hair growth laser device FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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Single Use

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Implantable

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Contains Latex

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Prescription Use

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Over-the-Counter

Yes

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Convenience Kit

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Combination Product

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HCT/P

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Premarket Exempt

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Lot / Batch Number

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Serial Number

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Expiration Date

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Manufacturing Date

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Category: Hair growth laser device

Revian Inc. Replacement Kit USB-C Power Cable by Revian, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K173729 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: Revian, Inc.

Sources (1)

FDA UDI 79e0047d-eba8-43e6-880d-e6349d1744cd 37 fields · synced May 31, 2026