Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015542970

FEI Number

3015542970

Entity Name

BIONIKS

City/State/Country

Alameda, CA, US

Establishment Address

2156 Central Avenue, Alameda, CA 94501, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Bioniks (Owner Number: 10060822)

Owner / Operator Contact Address

2156 Central Avenue, Alameda, CA 94501, 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
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2019-06-27

Official Correspondent

Louis Cheng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bioniks

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 3015542970. Last updated year: 2026. Please use registration number 3015542970 when referencing this establishment in official correspondence.