SOLEETECH CORPORATION

FDA Device Registration & Listing · Lujhou Taipei, TW · Registration 3003481016

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
3003481016
FEI Number
3003481016
Entity Name
SOLEETECH CORPORATION
City/State/Country
Lujhou Taipei, TW
Establishment Address
4F, No.4, Aly.24, Ln.227, Ming-zu Rd.,, Lujhou Taipei 247, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SOLEETECH CORPORATION (Owner Number: 10029739)
Owner / Operator Contact Address
4F, No.4, Aly.24, Ln.227, Ming-zu Rd.,, Lujhou, TW-TPE 247, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Apparatus, suction, operating-room, wall vacuum Tubing, Pressure and accessories Connector, airway (Extension) Nose clip Airway, oropharyngeal, anesthesiology

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered General Hospital Class 2 880.6740 2009-06-22
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 2009-06-22
CAM Yoke Assembly, Medical Gas Anesthesiology Class 1 868.6885 2009-06-22
BZA Connector, Airway (Extension) Anesthesiology Class 1 868.5810 2009-06-22
BXJ Clip, Nose Anesthesiology Class 1 868.6225 2009-06-22
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2009-06-22

Official Correspondent

No official correspondent registered.

US Agent Details

Daihong Ren Business: Sunrise Medical International Inc Email: sunrisemed1@gmail.com Phone: (765) 5131789

Related Public Records

Same Entity

SOLEETECH CORPORATION
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
K780365 Spica, Inc. OXYGEN/NITROUS OXIDE OUTLET 1978-03-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003481016. Last updated year: 2026. Please use registration number 3003481016 when referencing this establishment in official correspondence.
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