Lief Device Facility

FDA Device Registration & Listing · Berkeley, CA, US · Registration 3015542403

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
3015542403
FEI Number
3015542403
Entity Name
Lief Device Facility
City/State/Country
Berkeley, CA, US
Establishment Address
2703 7th Street, Suite #301, Mailbox #123, Berkeley, CA 94710, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Zenso, Inc. (Owner Number: 10060541)
Owner / Operator Contact Address
2443 Fillmore St #380-6060, San Francisco, CA 94115, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lief Rx

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2019-05-23

Official Correspondent

William Frese

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Zenso, Inc.
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 3015542403. Last updated year: 2026. Please use registration number 3015542403 when referencing this establishment in official correspondence.
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