FROGFISH INTERNATIONAL CORP.

FDA Device Registration & Listing · Taipei City, TW · Registration 3015173437

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
3015173437
FEI Number
3015173437
Entity Name
FROGFISH INTERNATIONAL CORP.
City/State/Country
Taipei City, TW
Establishment Address
No. 168, Jingye 3rd Road, Zhongshan District, Taipei City 10466, TW
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Frogfish International Corp. (Owner Number: 10059579)
Owner / Operator Contact Address
No. 168, Jingye 3rd Road, Zhongshan District, Taipei City, TW-NOTA 10466, TW
Initial Importer Flag
N
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
FQM Bandage, Elastic General Hospital Class 1 880.5075 2019-02-01
IQQ Joint, Shoulder, External Limb Component Physical Medicine Class 1 890.3420 2019-02-01
EFN Cotton, Roll Dental Class 1 872.6050 2019-02-01
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2019-02-01
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2019-02-01
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2019-02-01

Official Correspondent

Patrick Huang

US Agent Details

Kyle Davis Business: Modus Light, LLC Email: kyle.davis@moduslight.com Phone: (913) 2837753

Related Public Records

Same Entity

Frogfish International 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-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015173437. Last updated year: 2026. Please use registration number 3015173437 when referencing this establishment in official correspondence.
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