Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004450679

FEI Number

3004450679

Entity Name

INTAI TECHNOLOGY CORP.

City/State/Country

TAICHUNG CITY, TW

Establishment Address

9 JINGKE ROAD, NANTUN DISTRICT, TAICHUNG CITY 40852, TW

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

INTAI TECHNOLOGY CORP. (Owner Number: 9070084)

Owner / Operator Contact Address

9 JINGKE ROAD, NANTUN DISTRICT, TAICHUNG CITY, TW-TXG 40852, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EMF	Knife, Surgical	General, Plastic Surgery	Class 1	878.4800	2005-02-04
GAG	Stapler, Surgical	General Hospital	Class 2	878.4740	2017-07-31
MTD	Catheter, Intracardiac Mapping, High-Density Array	Cardiovascular	Class 2	870.1220	2022-04-06

Official Correspondent

No official correspondent registered.

US Agent Details

Jeff Liao Business: AOLTEC INTERNATIONAL, INC. Email: jeffliao@mail.aoltec.com Phone: (909) 6052700

Related Public Records

Same Entity

INTAI TECHNOLOGY CORP.

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
K221629	Covidien	Tri-Staple 2.0 Black Circular Reloads (for use with Signia Circular Adapters)	2023-02-22
K231491	Covidien	TA Stapler and Loading Unit with DST Series Technology	2023-08-16
K241372	ABBOTT MEDICAL	Advisor HD Grid X Mapping Catheter, Sensor Enabled	2024-07-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0070-2019	COVIDIEN LLC	2	EEA Circular Stapler with Tri-Staple Technology, Part No. TRIEEA28MT TRIEEA28XT TRIEEA31MT TRIEEA31XT Product Usage: The EEA Circular Stapler with Tri-Staple Technology places a circular, triple staggered row of titanium staples and resects the excess tissue, creating a circular anastomosis.

Similar Registrations

Registration Number	Establishment Name	Location
3009703496	DADDY D PRO	Sialkot Punjab, PK
2084346	MARINA MEDICAL INSTRUMENTS, INC.	Davie, FL, US
1720747	SONTEC INSTRUMENTS, INC.	CENTENNIAL, CO, US
3032391	Medline ReNewal	Redmond, OR, US
3011625373	METRO MEDICAL	Sialkot Punjab, PK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004450679. Last updated year: 2026. Please use registration number 3004450679 when referencing this establishment in official correspondence.