2M USB Magnetic Cable v2 Only Replacement Kit

FDA UDI

Class II (US FDA UDI)

by Revian, Inc.

Identity

Trade Name: 2M USB Magnetic Cable v2 Only Replacement Kit FDA UDI
Generic Name: Hair growth laser device FDA UDI
Device Name: The 2M USB Magnetic Cable v2 Only Replacement Kit is a kit that may be shipped to users of the REVIAN Red device (Catalog #10001) who have lost or misplaced their Magnetic Micro-USB Cable originally supplied with the REVIAN Red Device. FDA UDI
Model / Reference: 10000-12720 FDA UDI
Description: The 2M USB Magnetic Cable v2 Only Replacement Kit is a kit that may be shipped to users of the REVIAN Red device (Catalog #10001) who have lost or misplaced their Magnetic Micro-USB Cable originally supplied with the REVIAN Red Device. FDA UDI

Identifiers

Catalog Number: 12720 FDA UDI
Primary DI / UDI-DI: 00850003374116 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

FDA UDI

Single Use

FDA UDI

Implantable

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Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

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

2M USB Magnetic Cable v2 Only Replacement Kit 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 e894d234-a7c2-485a-92a5-9f6aaef2854d 37 fields · synced May 31, 2026