Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034211167

FEI Number

3034211167

Entity Name

CHENG HON PLASTIC ENTERPRISE CO., LTD.

City/State/Country

Kaohsiung City, TW

Establishment Address

No. 19, Daren St., Daliao Vil., Daliao Dist., Kaohsiung City 83160, TW

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Cheng Hon Plastic Enterprise Co., Ltd. (Owner Number: 10092047)

Owner / Operator Contact Address

No. 19, Daren St., Daliao Vil., Daliao Dist., Kaohsiung City, TW-KHH 83160, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

HolstOR PRO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2024-11-28

Official Correspondent

YAO-SHENG CHIANG

US Agent Details

Ho Shan Wang Email: acmebiotechs@gmail.com Phone: (623) 9864377

Related Public Records

Same Entity

Cheng Hon Plastic Enterprise Co., Ltd.

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 3034211167. Last updated year: 2026. Please use registration number 3034211167 when referencing this establishment in official correspondence.