Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024026674

FEI Number

3024026674

Entity Name

ANESTEK CORP.

City/State/Country

Taoyuan City, TW

Establishment Address

9F, No. 896, Jingguo Rd., Taoyuan City 33858, TW

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Anestek Corp. (Owner Number: 10085949)

Owner / Operator Contact Address

9F, No. 896, Jingguo Rd., Taoyuan City, TW-TAO 33858, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Laryn-Go Mini system, Laryn-Go Pro system, Laryn-Go Max system Disposable sheath (Sterilized): AT-SH25; AT-SH38; AT-SH49 Stylet-Go Mini system, Stylet-Go Pro system, Stylet-Go Max system Stylet-Go Mini Plus system, Stylet-Go Pro Plus system, Stylet-Go Max Plus system Flex-Go Mini System, Flex-Go Pro System, Flex-Go Max System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2022-09-19
BSR	Stylet, Tracheal Tube	Anesthesiology	Class 1	868.5790	2022-09-19
CAL	Laryngoscope, Non-Rigid	Anesthesiology	Class 1	868.5530	2024-04-01

Official Correspondent

Sy-Ming Guu

US Agent Details

Lily Lin Email: iesmguu@anestek.com.tw Phone: (314) 6680697

Related Public Records

Same Entity

Anestek Corp.

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-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3024026674. Last updated year: 2026. Please use registration number 3024026674 when referencing this establishment in official correspondence.