Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011006318

FEI Number

3011006318

Entity Name

AxoGen Corporation

City/State/Country

Burleson, TX, US

Establishment Address

300 Boone Rd Ste A3, Burleson, TX 76028, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AxoGen Corporation (Owner Number: 10031236)

Owner / Operator Contact Address

13631 Progress Blvd, Suite 400, Alachua, FL 32615, US

Initial Importer Flag

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
3017860045	Axogen Corporation - Tampa Heights	Tampa, FL, US

Similar Registrations

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3012669262	ALAFAIR BIOSCIENCES, INC.	Austin, TX, US
3025664014	KESSEL MEDICAL	Vero Beach, FL, US
2249852	COLLAGEN MATRIX, INC.	Oakland, NJ, US
3017860045	Axogen Corporation - Tampa Heights	Tampa, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011006318. Last updated year: 2026. Please use registration number 3011006318 when referencing this establishment in official correspondence.