Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9610410

FEI Number

3002806673

Entity Name

OKAMOTO RUBBER PRODUCTS CO., LTD.

City/State/Country

PATHUMTHANI Pathum Thani, TH

Establishment Address

60/50, 60/51 Moo 19, NAVANAKORN IND. ESTATE, ZONE 2, KLONGLUANG, PATHUMTHANI Pathum Thani 12120, TH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

OKAMOTO RUBBER PRODUCTS CO., LTD. (Owner Number: 9063116)

Owner / Operator Contact Address

60/50 NAVANAKORN, INDUSTRIAL ESTATE ZONE 2, KLONGLUANG PATHUMTHANI, TH-NOTA 12120, TH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K141256

PMA Number

N/A

All Registered Proprietary Names

Crown Condom WINK CLOSER WINK Studded

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2007-11-07
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2025-07-28
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2014-08-26

Official Correspondent

No official correspondent registered.

US Agent Details

Hisayuki Naito Business: Okamoto U.S.A., Inc. Email: okamotousa@okamotousa.com Phone: (203) 3780003

Related Public Records

Same Entity

OKAMOTO RUBBER PRODUCTS CO., LTD.

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9610410. Last updated year: 2026. Please use registration number 9610410 when referencing this establishment in official correspondence.