ASSISTIVE TECHNOLOGY DEVELOPMENT, INC.

FDA Device Registration & Listing · Orange, CA, US · Registration 3036496409

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
3036496409
FEI Number
3036496409
Entity Name
ASSISTIVE TECHNOLOGY DEVELOPMENT, INC.
City/State/Country
Orange, CA, US
Establishment Address
2029 W Orangewood Ave Ste B, Orange, CA 92868, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Assistive Technology Development, Inc. (Owner Number: 10092975)
Owner / Operator Contact Address
2029 W. Orangewood Ave., Suite B, Orange, CA 92868, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Reflex Reflex KN33-LE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKK System, Isokinetic Testing And Evaluation Physical Medicine Class 2 890.1925 2025-03-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Assistive Technology Development, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036496409. Last updated year: 2026. Please use registration number 3036496409 when referencing this establishment in official correspondence.
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