Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013849323

FEI Number

3013849323

Entity Name

KONO SEISAKUSHO

City/State/Country

Ichikawa Chiba, JP

Establishment Address

Soya 2-11-10, Ichikawa Chiba 272-0832, JP

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Kono Seisakusho (Owner Number: 10077957)

Owner / Operator Contact Address

Soya 2-11-10, Ichikawa, JP-12 272-0832, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PICOCLAMP CROWNJUN Micro Sheet K CROWNJUN Super Micro Sheet K CROWNJUN Micro Scale Single Retractor Double Retractor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2023-11-10
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2022-09-25
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2023-02-20

Official Correspondent

Hiroyuki Arai

US Agent Details

Max Sturgis Business: Mitaka USA Email: max@mitakausa.com Phone: (720) 7729110

Related Public Records

Same Entity

Kono Seisakusho

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
K922626	Andronic Devices, Ltd.	ADEPT INSTRUMENT POSITIONING ACCESSORY	1992-10-19
K820290	The Anspach Effort, Inc.	SELF RETAINING RETRACTOR FOR HAND SURG	1982-03-05
K760422	Cutter Laboratories, Inc.	SURGICAL RETRACTOR	1976-08-23

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2014	Aesculap, Inc.	1	UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

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1055236	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US
2950160	WRIGHT ENGINEERED PLASTICS, INC.	Santa Rosa, CA, US
3005809810	Jarit GmbH	Rietheim-Weilheim Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013849323. Last updated year: 2026. Please use registration number 3013849323 when referencing this establishment in official correspondence.