Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027256314

FEI Number

3027256314

Entity Name

APPSCENT MEDICAL

City/State/Country

Raanana Central, IL

Establishment Address

15 HaTidhar Street, Raanana Central 4366517, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Appscent Medical (Owner Number: 10090767)

Owner / Operator Contact Address

15 HaTidhar Street, Raanana, IL-M 4366517, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Scentific Test Kit SCENTIFIC Respiratory Biofeedback

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NRK	Kit, Test, Olfactory	Ear, Nose, Throat	Class 2	874.1600	2024-05-10
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2025-07-10

Official Correspondent

Saray Gani

US Agent Details

Mindy McCann Business: Qserve Group US Inc. Email: USagent@Qservegroup.Com Phone: (424) 2718169

Related Public Records

Same Entity

Appscent Medical

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027256314. Last updated year: 2026. Please use registration number 3027256314 when referencing this establishment in official correspondence.