KINETIC RESEARCH

FDA Device Registration & Listing · Tampa, FL, US · Registration 3008306818

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
3008306818
FEI Number
3008306818
Entity Name
KINETIC RESEARCH
City/State/Country
Tampa, FL, US
Establishment Address
5513 West Sligh Ave, Tampa, FL 33634, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kinetic Research (Owner Number: 10031183)
Owner / Operator Contact Address
5513 West Sligh Ave, Tampa, FL 33634, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

The Noodle AFO MaxForce AFO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2009-12-30
ISH Component, External, Limb, Ankle/Foot Physical Medicine Class 1 890.3420 2015-04-24

Official Correspondent

Reid Bader

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kinetic Research
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 3008306818. Last updated year: 2026. Please use registration number 3008306818 when referencing this establishment in official correspondence.
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