Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030624673

FEI Number

3030624673

Entity Name

DARMIYAN, INC.

City/State/Country

Campbell, CA, US

Establishment Address

900 E Hamilton Ave, Suite 100, Campbell, CA 95008, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Darmiyan, Inc. (Owner Number: 10085952)

Owner / Operator Contact Address

900 E Hamilton Ave, Suite 100, Campbell, CA 95008, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BrainSee

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QWT	Prognostic Assessment Software Of Mild Cognitive Impairment	Neurology	Class 2	882.1454	2024-03-18

Official Correspondent

Pavan Krishnamurthy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Darmiyan, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3028606342	OMAY(GUANGZHOU) MED TECHNOLOGIES CO., LTD	Guangzhou Guangdong, CN
3038274470	BRAINMATTERZ, INC	McKinney, TX, US
3012404174	LABORATORIO CHIMICO FARMACEUTICO A. SELLA SRL.	Schio Vicenza, IT
3042364673	NEURALYTIX LLC	Fruita, CO, US
3043617526	AD SCIENTIAM	Paris Ile-de-France, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030624673. Last updated year: 2026. Please use registration number 3030624673 when referencing this establishment in official correspondence.