MEGAFORCE COMPANY LIMITED

FDA Device Registration & Listing · New Taipei City, TW · Registration 3016750643

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016750643
FEI Number
3016750643
Entity Name
MEGAFORCE COMPANY LIMITED
City/State/Country
New Taipei City, TW
Establishment Address
1-2F., No.5 & 7, Ziqiang St.,Tucheng Dist., New Taipei City 23678, Taiwan (R.O.C.), New Taipei City 236, TW
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MEGAFORCE COMPANY LIMITED (Owner Number: 10068151)
Owner / Operator Contact Address
1-2F., No.5 & 7, Ziqiang St.,Tucheng Dist., New Taipei City 23678, Taiwan (R.O.C.), New Taipei City, TW-TPE 236, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Surgi box CTU138-2; Neck Air Traction Device CTU359; CTU366; Cervical Traction Unit KEGG SMOLTAP Infant Stabilizer; SMOLTAP Infant Stabilizer Face Pad; SMOLTAP Infant Stabilizer Straps

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FZI Apparatus, Air Handling, Enclosure General, Plastic Surgery Class 2 878.5070 2026-04-29
HST Apparatus, Traction, Non-Powered Orthopedic Class 1 888.5850 2024-05-03
NGE Test, Luteinizing Hormone (Lh), Over The Counter Clinical Chemistry Class 1 862.1485 2020-04-08
PRN Pediatric Position Holder General Hospital Class 1 880.5680 2022-08-23

Official Correspondent

Eric Chen

US Agent Details

Wei-Chun Chin Email: weichun.chin@gmail.com Phone: (209) 2288668

Related Public Records

Same Entity

MEGAFORCE COMPANY LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0043-2024 Universal Meditech Inc. 1
One Step Ovulation Test REF 200-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016750643. Last updated year: 2026. Please use registration number 3016750643 when referencing this establishment in official correspondence.
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