Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009522766

FEI Number

3009522766

Entity Name

CUREXO, Inc.

City/State/Country

Songpa-gu Seoul, KR

Establishment Address

3rd/4th Fl., 480, Wiryesunhwan-ro, Songpa-gu Seoul 05814, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Curexo Inc. (Owner Number: 10053880)

Owner / Operator Contact Address

3rd, 4th Fl., 480, Wiryesunhwan-ro, Songpa-gu, Seoul, KR-11 05814, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K252037

PMA Number

N/A

All Registered Proprietary Names

Morning Walk Gait Rehabilitation Robot System MW-S200 MW-S200C CUVIS-spine CUVIS-spine CUVIS-spine CUVIS-joint(CJ150)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKK	System, Isokinetic Testing And Evaluation	Physical Medicine	Class 2	890.1925	2017-01-19
OLO	Orthopedic Stereotaxic Instrument	Neurology	Class 2	882.4560	2022-10-25
OLO	Orthopedic Stereotaxic Instrument	Neurology	Class 2	882.4560	2023-06-24
OLO	Orthopedic Stereotaxic Instrument	Neurology	Class 2	882.4560	2021-05-24
OLO	Orthopedic Stereotaxic Instrument	Neurology	Class 2	882.4560	2026-04-07

Official Correspondent

Gwijeong Lee

US Agent Details

Joyce Kwon Business: Provision Consulting Group, Inc. Email: ask@provisionfda.com Phone: (909) 4933276

Related Public Records

Same Entity

Curexo Inc.

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
K260601	Blue Belt Technologies, Inc.	REAL INTELLIGENCE CORI	2026-03-26

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0041-2024	Blue Belt Technologies, Inc	2	Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009522766. Last updated year: 2026. Please use registration number 3009522766 when referencing this establishment in official correspondence.