BERTEC CORP.

FDA Device Registration & Listing · COLUMBUS, OH, US · Registration 1530895

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
1530895
FEI Number
1000480800
Entity Name
BERTEC CORP.
City/State/Country
COLUMBUS, OH, US
Establishment Address
2500 Citygate Drive, COLUMBUS, OH 43219, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BERTEC CORPORATION (Owner Number: 9033991)
Owner / Operator Contact Address
2500 Citygate Drive, --, Columbus, OH 43219, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bertec Vision Trainer System (BVT) Bertec Vision Trainer System (BVT)

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 2022-01-21
PTY Computerized Cognitive Assessment Aid, Exempt Neurology Class 2 882.1470 2022-01-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BERTEC CORPORATION
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 1530895. Last updated year: 2026. Please use registration number 1530895 when referencing this establishment in official correspondence.
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