Axogen Corporation - Tampa Heights

FDA Device Registration & Listing · Tampa, FL, US · Registration 3017860045

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
3017860045
FEI Number
3017860045
Entity Name
Axogen Corporation - Tampa Heights
City/State/Country
Tampa, FL, US
Establishment Address
111 W Oak Ave, Suite 500, Tampa, FL 33602, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
AxoGen Corporation (Owner Number: 10031236)
Owner / Operator Contact Address
13631 Progress Blvd, Suite 400, Alachua, FL 32615, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K231708
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JXI Cuff, Nerve Neurology Class 2 882.5275 2017-10-04
JXI Cuff, Nerve Neurology Class 2 882.5275 2023-11-13

Official Correspondent

Jesse Bishop

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AxoGen Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011006318 AxoGen Corporation Burleson, TX, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017860045. Last updated year: 2026. Please use registration number 3017860045 when referencing this establishment in official correspondence.
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