YUWA SEISAKUSHO KK

FDA Device Registration & Listing · Odawara Kanagawa, JP · Registration 3008998088

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
3008998088
FEI Number
3008998088
Entity Name
YUWA SEISAKUSHO KK
City/State/Country
Odawara Kanagawa, JP
Establishment Address
2136 Michishita, Kayama, Odawara Kanagawa 250-0852, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Yuwa Seisakusho KK (Owner Number: 10036140)
Owner / Operator Contact Address
2136 Michishita, Kayama, Odawara, JP-14 250-0852, JP
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
ECI Band, Elastic, Orthodontic Dental Class 1 872.5410 2011-04-21

Official Correspondent

Hiroki Honna

US Agent Details

Randy Burhans Business: Phoenix Orthodontics Inc. Email: randy@phoenixorthoga.com Phone: (770) 6438896

Related Public Records

Same Entity

Yuwa Seisakusho KK
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-0012-2012 Biomet Microfixation, Inc. 1
Biomet Microfixation outer packaging labeled in part:"REF: SP-2411***RUBBER BAND, LATEX FREE SMALL, HEAVY, 300/PACKAGE 4MM, (3/16" INNER DIAMETER) NON LATEX ELASTICS LOT 307850***DISTRIBUTED BY: BIOMET MICROFIXATION 1520 Tradeport Drive, Jacksonville, FL 32218 USA www.biometmicrofixation.com***." Inner Vendor/Manufacturer Label labeled in part:"H4 Elastics 4mm (3/16") Heavy 4 oz. REF 11-102-04***Manufactured for DENTSPLY GAC INTERNATIONAL DENTSPLY INTERNATIONAL, INC. Phone 631-419-1700 Fax 631-419-1599 355 Knickerbocker Avenue Bohemia NY 11716 USA***MediMark Europe BP2332 F-38033 Grenoble Cedex 2. France***LOT 82936-32 QTY:100 pk use by 2012-07 Made in USA ISSUED DATE 2009-04 GN***" Elastic bands used as elastomeric ties for ligation that facilitate treatment of fracture of the mandible and maxilla. They are commonly used with braces or arch bar wire.

Similar Registrations

Registration Number Establishment Name Location
3008005217 US ORTHODONTIC PRODUCTS Norwalk, CA, US
3009491780 Phoenix Orthodontics Inc Marietta, GA, US
1833132 G & H Wire Company Franklin, IN, US
9611458 Dentaurum GmbH & Co. KG ISPRINGEN Baden-Wurttemberg, DE
3022296393 FIRST DENTAL SUPPLIES LLC Winter Garden, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008998088. Last updated year: 2026. Please use registration number 3008998088 when referencing this establishment in official correspondence.
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