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INTAI TECHNOLOGY CORP.

鐿鈦科技股份有限公司

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2004Founded
NT$507MPaid-in capital
3Plants
38Certifications
10Patents
NT$0.5–1BRevenue band (est.)
Unified Business No.
27473348
Industry
Fabricated Metal Products (25,390)
Main products
Other fabricated metal products (10,961)
Location
NO. 9, JINGKE RD., NANTUN DIST., TAICHUNG CITY, TAIWAN (R.O.C.)
Taichung City (17,121) · Nantun Dist. (433)
Listing
Listed (TPEx) (890) 4163
Registration status
Approved / Active
Organisation type
Company Limited by Shares
Founded
2004-10-21
Paid-in capital
NT$ 506,796,430
Representative
Chung Chao-hsun
Phone
04-23595336
Website
http://ir.intai.com.tw/
Exporter
Yes — registered with the Trade Administration
Annual revenue band
NT$0.5–1B estimated
Ownership
Group subsidiary / corporate-held · Yi Fa Co., Ltd.、Hung Wei Tou Tzu Co., Ltd.、Chih Chia Tou Tzu Co., Ltd.
North American market
FDA 510(k) clearance FDA medical device registration
Representative tenure
In office since 2020-07 (6 yrs); last handover 2020-07
Growth & profitability
Revenue 2026-09 YoY +18.0%, year-to-date +13.9%
Gross margin 42.2%, operating margin 12.2%, net margin 10.9% (2026-Q2 YTD)
Compliance record
FDA import refusal: 1 product(s), latest 2024-07-30
Environmental penalties: 7 case(s) in 5 years, latest 2024-08-29, fines NT$ 1,000,000 (stationary air pollution; industrial waste; water pollution)
Occupational safety penalties: 1 case(s) in 5 years, latest 2025-05-14 (Art. 6) — matched by company name

Plants 3

Certifications 38

Processes & materials 11

Patents 10

  • 2026 90 GHz liquid crystal millimeter-wave switch structure
  • 2025 Motor actuator with sealing and pressure balance
  • 2024 Control system for hydraulic power steering device

North American market evidence 6

  • FDA 510(k) clearance K210422 2022-03-30
    INTAI Surgical Mask (non-sterile)
  • FDA 510(k) clearance K201229 2022-03-11
    Intai Anatomic Locking Plate and Screw System
  • FDA 510(k) clearance K180523 2019-09-20
    INTAI Surgery Navigation System
  • FDA 510(k) clearance K122804 2013-05-20
    ROYAL-DENT EUREKA DENTAL IMPLANT SYSTEM
  • FDA medical device registration 3004450679 2005-02-04 – 2026-08-19
    Stapler, Surgical; Endoscopic Tissue Approximation Device; Knife, Surgical and more (5)
  • FDA import refusal 3004450679 2023-04-18 – 2024-07-30
    SCREW, FIXATION, BONE

Recent changes 3

  • Certification expiry · UpcomingMedical device license (Class II) certificate expires on 2027-01-27
  • Certification expiry · UpcomingMedical device license (Class I) certificate expires on 2027-01-18
  • Certification expiryMedical device license (Class II) certificate expired on 2026-05-14

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