SHIKEN CORPORATION

FDA Device Registration & Listing · KOMATSUSHIMA Tokushima, JP · Registration 3010331033

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
3010331033
FEI Number
3010331033
Entity Name
SHIKEN CORPORATION
City/State/Country
KOMATSUSHIMA Tokushima, JP
Establishment Address
55-1, AZANISHIIYASHIKI, SHIBOUCHOU, KOMATSUSHIMA Tokushima 773-0009, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SHIKEN CORPORATION (Owner Number: 10091032)
Owner / Operator Contact Address
55-1, AZANISHIIYASHIKI, SHIBOUCHOU, KOMATSUSHIMA, JP-36 773-0009, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dentures, partial Restoration, porcelain Dentures, full

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSP Restoration, Porcelain Unknown Class N N/A 2024-10-30

Official Correspondent

Takahiro Shima

US Agent Details

Nathan Gallinger Business: Quest Dental USA Corp Email: nathan-gallinger@quest-pure.com Phone: (949) 8703985

Related Public Records

Same Entity

SHIKEN CORPORATION
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 3010331033. Last updated year: 2026. Please use registration number 3010331033 when referencing this establishment in official correspondence.
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