MatPLUS, LTD

FDA Device Registration & Listing · Painesville, OH, US · Registration 3003653126

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
3003653126
FEI Number
3003653126
Entity Name
MatPLUS, LTD
City/State/Country
Painesville, OH, US
Establishment Address
76 Burton St, Painesville, OH 44077, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
MatPLUS LTD (Owner Number: 10037844)
Owner / Operator Contact Address
76 Burton St, Painesville, OH 44077, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Thera Series Brace Post-Op Wedge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYS Insoles, Medical General Hospital Class 1 880.6280 2017-10-24
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2017-10-24
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2017-10-24

Official Correspondent

System Admin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MatPLUS LTD
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 3003653126. Last updated year: 2026. Please use registration number 3003653126 when referencing this establishment in official correspondence.
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