Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003969012

FEI Number

3003969012

Entity Name

Alltion (Guangxi) Instrument Co., Ltd.

City/State/Country

Wuzhou City Guangxi, CN

Establishment Address

No.10, 3rd Road, Wuzhou Industrial Park, Wuzhou City Guangxi 543000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Alltion (Wuzhou) Co., Ltd. (Owner Number: 9055212)

Owner / Operator Contact Address

No.10, 3rd Road, Wuzhou Industrial Park, Wuzhou City, CN-GX 543000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LOUPE, DIAGNOSTIC/SURGICAL Colposcope (and Colpomicroscope) AC-3300 Colposcope AC-5000 Colposcope AC-3500 Colposcope Microscope, Operating & Accessories, AC-Powered, Ophthalmic Light, Microscope Headlamp, Operating, Battery-Operated

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSP	Loupe, Diagnostic/Surgical	General, Plastic Surgery	Class 1	878.4800	2007-04-13
HEX	Colposcope (And Colpomicroscope)	Obstetrics/Gynecology	Class 2	884.1630	2007-04-13
PTZ	Colposcope (And Colpomicroscope), Exempt	Obstetrics/Gynecology	Class 2	884.1630	2022-12-28
HRM	Microscope, Operating & Accessories, Ac-Powered, Ophthalmic	General, Plastic Surgery	Class 1	878.4700	2003-02-21
IBJ	Light, Microscope	Pathology	Class 1	864.3600	2008-05-08
HPP	Headlamp, Operating, Battery-Operated	Ophthalmic	Class 1	886.4335	2007-04-13

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Alltion (Wuzhou) Co., Ltd.

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 3003969012. Last updated year: 2026. Please use registration number 3003969012 when referencing this establishment in official correspondence.