CURACO INC

FDA Device Registration & Listing · Seongnam-si Gyeonggi, KR · Registration 3011094311

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
3011094311
FEI Number
3011094311
Entity Name
CURACO INC
City/State/Country
Seongnam-si Gyeonggi, KR
Establishment Address
#410, 172 Dolma-ro, Bundang-gu, Seongnam-si Gyeonggi 13605, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Curaco Inc (Owner Number: 10047153)
Owner / Operator Contact Address
#410, 172 Dolma-ro, Bundang-gu, Seongnam-si, KR-41 13605, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Carebidet Carebidet Carebidet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDP Regulator, Vacuum General Hospital Class 2 880.6740 2014-07-08
JOL Catheter And Tip, Suction General Hospital Class 2 880.6740 2014-07-08
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2014-07-08

Official Correspondent

Hoonsang Lee

US Agent Details

Wonwoo Suh Business: HS Chem America Email: mjk11@hotmail.com Phone: (213) 5597719

Related Public Records

Same Entity

Curaco Inc
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-0007-2013 Invuity, Inc. 2
BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011094311. Last updated year: 2026. Please use registration number 3011094311 when referencing this establishment in official correspondence.
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