Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016248620

FEI Number

3016248620

Entity Name

PSYONIC

City/State/Country

San Diego, CA, US

Establishment Address

10949 Technology Pl Ste A, San Diego, CA 92127, US

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

PSYONIC (Owner Number: 10062014)

Owner / Operator Contact Address

10949 Technology Place, Suite A, San Diego, CA 92127, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ability Hand

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQZ	Hand, External Limb Component, Powered	Physical Medicine	Class 1	890.3420	2019-12-11

Official Correspondent

Aadeel Akhtar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PSYONIC

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 3016248620. Last updated year: 2026. Please use registration number 3016248620 when referencing this establishment in official correspondence.