PERRY DYNAMICS, INC.

FDA Device Registration & Listing · Decatur, IL, US · Registration 3004979815

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
3004979815
FEI Number
3004979815
Entity Name
PERRY DYNAMICS, INC.
City/State/Country
Decatur, IL, US
Establishment Address
3221 N Woodford St., Decatur, IL 62526, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Perry Dynamics, Inc. (Owner Number: 10030854)
Owner / Operator Contact Address
3221 N Woodford St., Decatur, IL 62526, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PROPRIO 5000 PROPRIO 3000

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 2009-11-18

Official Correspondent

Joe Perry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Perry Dynamics, 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 3004979815. Last updated year: 2026. Please use registration number 3004979815 when referencing this establishment in official correspondence.
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