STONER INCORPORATED

FDA Device Registration & Listing · Quarryville, PA, US · Registration 3000538043

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
3000538043
FEI Number
3000538043
Entity Name
STONER INCORPORATED
City/State/Country
Quarryville, PA, US
Establishment Address
1070 Robert Fulton Hwy, Quarryville, PA 17566, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Stoner Incorporated (Owner Number: 10053039)
Owner / Operator Contact Address
1070 Robert Fulton Highway, Quarryville, PA 17566, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAT Tester, Pulp Dental Class 2 872.1720 2016-10-25
ECN Clamp, Wire, Orthodontic Dental Class 1 872.5410 2016-10-25

Official Correspondent

Robert Sweger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stoner Incorporated
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 3000538043. Last updated year: 2026. Please use registration number 3000538043 when referencing this establishment in official correspondence.
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