Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8031680

FEI Number

3003135788

Entity Name

SEIRIN CORPORATION

City/State/Country

SHIZUOKA-SHI, JP

Establishment Address

147 Ouchi, SHIMIZU-KU, SHIZUOKA-SHI 424-0061, JP

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

SEIRIN CORPORATION (Owner Number: 8031680)

Owner / Operator Contact Address

147 Ouchi, SHIMIZU-KU, SHIZUOKA, JP-22 424-0061, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

D-type(Dtype SP) L-Type J15 J15 (J-Sakura) ELIPEAS D-Type Pyonex L-Type (L-Tsubaki) G-Type J-type (JSP type) KB-Type D-Type (D-Kaede) J-Type M-Type J15(J15SP type) Spinex J ProPak10 J-Type (J-Sakura) B-Type L-type(Ltype SP) G-type(Gtype SP) SEIRIN MOXSAFE - MOXSAFE 20; MOXSAFE 100

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2018-05-21
IMA	Pack, Heat, Moist	Physical Medicine	Class 1	890.5730	2010-08-31

Official Correspondent

No official correspondent registered.

US Agent Details

MATTHEW PIKE Business: SEIRIN-AMERICA, INC. Email: mpikeoms@aol.com Phone: (781) 3401827

Related Public Records

Same Entity

SEIRIN CORPORATION

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 8031680. Last updated year: 2026. Please use registration number 8031680 when referencing this establishment in official correspondence.