REVIAN, Inc

FDA Device Registration & Listing · Morrisville, NC, US · Registration 3015249767

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015249767
FEI Number
3015249767
Entity Name
REVIAN, Inc
City/State/Country
Morrisville, NC, US
Establishment Address
615 Davis Dr Ste 800, Morrisville, NC 27560, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
REVIAN, Inc. (Owner Number: 10059863)
Owner / Operator Contact Address
615 Davis Drive, Suite 800, Morrisville, NC 27560, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Replacement Kit, 120V AC-5VDC 2A Wall, Type A Plug (12707) USB-C Charging Cable Replacement Kit (12723) Replacement Kit, REVIAN 2M USB Magnetic Cable and Insert V2 (12722) REVIAN Headliner Replacement Kit - Universal (12600) Revian Red (10001) GetHairMD Hair Growth System (10013) Replacement Kit, REVIAN 2M USB Magnetic Cable V2 Only (12720)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OAP Laser, Comb, Hair Physical Medicine Class 2 890.5500 2019-03-21

Official Correspondent

Tammy Carrea

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

REVIAN, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015249767. Last updated year: 2026. Please use registration number 3015249767 when referencing this establishment in official correspondence.
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