Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030183061

FEI Number

3030183061

Entity Name

MIING WEI CO., LTD.

City/State/Country

Tsao-Twon Nantou, TW

Establishment Address

No. 211-38, Tsao Shi Rd., Tsao-Twon Nantou 542008, TW

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MIING WEI CO., LTD. (Owner Number: 10089083)

Owner / Operator Contact Address

No. 211-38, Caoxi Rd., Caotun, TW-NAN 542008, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SPINAL INSTRUMENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OCJ	Spinal Channeling Instrument, Vertebroplasty	Orthopedic	Class 1	888.4540	2025-11-20
HXX	Screwdriver	Orthopedic	Class 1	888.4540	2025-11-20
NDL	Pin, Fixation, Smooth, Metallic	Orthopedic	Class 2	888.3040	2025-11-20
HRS	Plate, Fixation, Bone	Orthopedic	Class 2	888.3030	2025-11-20
HWC	Screw, Fixation, Bone	Orthopedic	Class 2	888.3040	2025-11-20
HWX	Tap, Bone	Orthopedic	Class 1	888.4540	2025-11-20
EJB	Handle, Instrument, Dental	Dental	Class 1	872.4565	2025-11-20

Official Correspondent

LI YEN HOU

US Agent Details

Fan Lu Email: algaencorp@gmail.com Phone: (336) 5774354

Related Public Records

Same Entity

MIING WEI CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K042598	Zimmer, Inc.	PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES	2004-10-29
K190842	Jiangsu Trauhui Medical Instrument Co., Ltd.	Comus Locking Plate systems	2020-02-03
K130510	Arthrex, Inc.	ARTHREX COMPRESSION PLATES	2013-09-25
K202803	Newclip Technics	Activmotion S DTO	2021-12-16
K062348	Medtronic Neurosurgery	TIMESH SELF DRILLING SCREW	2006-09-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0034-2022	Flower Orthopedics Corporation	2	Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Z-0014-2014	Synthes USA HQ, Inc.	2	Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture, fixation, osteotomies, nonunions, and fusions of large bones in the foot and ankle.
Z-0026-2013	Orthohelix Surgical Designs Inc	2	OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the hand, wrist, afoot, and ankle.
Z-0026-2016	Ortho Solutions Inc 330 Franklin Tnpk	2	Ortho OS Solutions UltOS 3.5mm locking screw 12mm to 50mm Ortho Solutions LTD, Unit 5 West Station Business Park, Spital Road, Maldon, Essex CM96FF Rx Only a) Sterile b) Non-Sterile Orthopaedic Bone Screw
Z-0027-2013	Orthohelix Surgical Designs Inc	2	OrthoHelix Part #HCS-056-32 3.8MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the hand, wrist, afoot, and ankle.

Similar Registrations

Registration Number	Establishment Name	Location
3008583793	ZAVATION	Flowood, MS, US
3016789487	JIANGSU CHANGMEI MEDTECH CO.,LTD	Changzhou Jiangsu, CN
3013846070	GREENS SURGICALS PRIVATE LIMITED	Vadodara Gujarat, IN
3027518990	NINGBO HICREN BIOTECHNOLOGY CO., LTD.	Ningbo Zhejiang, CN
1220477	ISOMEDIX OPERATIONS INC.	Northborough, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030183061. Last updated year: 2026. Please use registration number 3030183061 when referencing this establishment in official correspondence.