STUDIO ARTS

FDA Device Registration & Listing · Easton, PA, US · Registration 3010197301

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
3010197301
FEI Number
3010197301
Entity Name
STUDIO ARTS
City/State/Country
Easton, PA, US
Establishment Address
4055 William Penn Highway, Easton, PA 18045, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Studio Arts (Owner Number: 10082426)
Owner / Operator Contact Address
4055 William Penn Highway, Easton, PA 18045, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Denture partial Denture full crown

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSK Dentures, Partial Unknown Class N N/A 2021-07-26
NSL Dentures, Full Unknown Class N N/A 2021-07-26
NSO Restoration, Porcelain-Fused-To-Metal Unknown Class N N/A 2021-07-26

Official Correspondent

Lorraine McGinley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Studio Arts
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 3010197301. Last updated year: 2026. Please use registration number 3010197301 when referencing this establishment in official correspondence.
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