Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019027610

FEI Number

3019027610

Entity Name

AEON BIOTHERAPEUTICS CORP.

City/State/Country

New Taipei City, TW

Establishment Address

1F. & 2F. No. 16, Ln. 658, Yingtao Rd. Yingge Dist., New Taipei City 23943, TW

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Aeon Biotherapeutics Corp. (Owner Number: 10086150)

Owner / Operator Contact Address

1F. & 2F. No. 16, Ln. 658, Yingtao Rd. Yingge Dist., New Taipei City, TW-NWT 23943, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
ORG	Platelet And Plasma Separator For Bone Graft Handling	Hematology	Class 2	864.9245	2024-03-18
KST	System, Blood Collection, Vacuum-Assisted, Manual	Hematology	Class 1	864.9125	2022-10-18

Official Correspondent

Shirley Ting

US Agent Details

Shih-Wei George Chen Email: info@theaeonglobal.com Phone: (858) 2083248

Related Public Records

Same Entity

Aeon Biotherapeutics Corp.

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 3019027610. Last updated year: 2026. Please use registration number 3019027610 when referencing this establishment in official correspondence.