Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000627797

FEI Number

1000627797

Entity Name

CHIKAMI MILTEC, INC.

City/State/Country

KOCHI, JP

Establishment Address

1961-1 Edagawa, Ino-cho, Agawa-gun, KOCHI 781-2120, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CHIKAMI MILTEC, INC. (Owner Number: 9044737)

Owner / Operator Contact Address

1-6-3 Ohtesuji, Kochi, JP-NOTA 780-0842, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

(RWS-P36, RWL-P36, RWS-P50, RWL-P50) (RWS-42, RWS-48, RWS-54, RWL-42, RWL-48, RWL-54, RWL-W50) Q.C.M. RETAINER WIRE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DZC	Wire, Orthodontic	Dental	Class 1	872.5410	2001-02-13

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

CHIKAMI MILTEC, 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
K112640	Ormco Corp.	HYPERELASTIC WIRE	2011-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000627797. Last updated year: 2026. Please use registration number 1000627797 when referencing this establishment in official correspondence.