Kalogon Inc

FDA Device Registration & Listing · Melbourne, FL, US · Registration 3017526035

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
3017526035
FEI Number
3017526035
Entity Name
Kalogon Inc
City/State/Country
Melbourne, FL, US
Establishment Address
300 North Dr Ste 106, Melbourne, FL 32934, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kalogon Inc. (Owner Number: 10081156)
Owner / Operator Contact Address
300 N Drive STE 106, Melbourne, FL 32934, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Orbiter Classic Verro Orbiter Med

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IMP Cushion, Wheelchair Physical Medicine Class 1 890.3920 2021-03-22

Official Correspondent

Timothy Balz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kalogon Inc.
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 3017526035. Last updated year: 2026. Please use registration number 3017526035 when referencing this establishment in official correspondence.
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