Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007608780

FEI Number

3007608780

Entity Name

OCHS LABS, LLC

City/State/Country

Sebastopol, CA, US

Establishment Address

7300 Healdsburg Avenue, Suite C, Sebastopol, CA 95472, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ochs Labs LLC (Owner Number: 10029376)

Owner / Operator Contact Address

7300 Healdsburg Avenue, Suite C, Sebastopol, CA 95472, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2009-05-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ochs Labs LLC

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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3038620647	KISO EHF	Reykjavik, IS
3005196642	HARMONIC ENERGETIC TECHNOLOGIES, LLC	Liverpool, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007608780. Last updated year: 2026. Please use registration number 3007608780 when referencing this establishment in official correspondence.