Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009758645

FEI Number

3009758645

Entity Name

NEOCHORD, INC

City/State/Country

Maple Grove, MN, US

Establishment Address

10900 73rd Ave N Ste 101, Maple Grove, MN 55369, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

NeoChord, Inc (Owner Number: 10043340)

Owner / Operator Contact Address

10900 73rd Ave North, Suite 101, Maple Grove, MN 55369, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DS1000

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PCX	Artificial Chordae Tendinae Delivery System	Unknown	Class N	N/A	2013-02-06

Official Correspondent

Kavitha Ganesan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeoChord, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009758645. Last updated year: 2026. Please use registration number 3009758645 when referencing this establishment in official correspondence.