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Revian Magnetic Micro-USB Connector Only Replacement Kit

FDA UDI

Class II (US FDA UDI)

by Revian, Inc.

Identity

Trade Name
Revian Magnetic Micro-USB Connector Only Replacement Kit FDA UDI
Generic Name
Hair growth laser device FDA UDI
Device Name
The Revian Magnetic Micro-USB Connector 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 Connector originally supplied with the REVIAN Red Device. FDA UDI
Model / Reference
10000-12718 FDA UDI
Description
The Revian Magnetic Micro-USB Connector 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 Connector originally supplied with the REVIAN Red Device. FDA UDI

Identifiers

Catalog Number
12718 FDA UDI
Primary DI / UDI-DI
00850003374093 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
Not 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Revian Magnetic Micro-USB Connector Only Replacement Kit by Revian, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Revian, Inc.

Sources (1)

  • FDA UDI 2431e66a-4955-40e6-9418-713042b4ea4a 38 fields · synced May 30, 2026