THE PETTIBON SYSTEM

FDA Device Registration & Listing · Chehalis, WA, US · Registration 3005033444

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
3005033444
FEI Number
3005033444
Entity Name
THE PETTIBON SYSTEM
City/State/Country
Chehalis, WA, US
Establishment Address
2118 JACKSON HWY, Chehalis, WA 98532, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
The Pettibon System, Inc (Owner Number: 9076299)
Owner / Operator Contact Address
2118 Jackson Hwy, Chehalis, WA 98532, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

The Pettibon System WOBBLE CHAIR-PLATFORM THE PETTIBON VIBRATION LINKED EXERCISE PETTIBON WOBBLE CHAIR Cervical Lordosis Posture Strap; 6-Way Cervical Dorsal Stretch Strap PETTIBON CERVICAL The Pettibon System PETTIBON TENDON MUSCL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2013-01-30
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2006-12-13
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 2005-08-11
IQK Orthosis, Cervical Physical Medicine Class 1 890.3490 2016-02-16
HST Apparatus, Traction, Non-Powered Orthopedic Class 1 888.5850 2005-08-11
IQE Orthosis, Lumbar Physical Medicine Class 1 890.3490 2016-02-16
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2005-08-11

Official Correspondent

Helene Pettibon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Pettibon System, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821133 Durham Electric Co. ELECTRICAL VIBRATING DEVICE 1982-07-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2025 Ossur H F Grjothals 5 Reykjavik Iceland 1
Miami J Select Collar, Catalog: MJS-101; Miami J Select Collar Set, Catalog: MJSR-101

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005033444. Last updated year: 2026. Please use registration number 3005033444 when referencing this establishment in official correspondence.
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