Manufacturer registered with FDA

Stoner Incorporated

Quarryville, PA, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10053039Contract manufacturerManufacturer
Device types listed
2
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Stoner Incorporated currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Pulp TesterEAT · Class 2—Maker—2016
Orthodontic Wire ClampECN · Class 1—Maker—2016

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
STONER INCORPORATEDFDA reg. 3000538043Quarryville, PA, United StatesContract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10053039). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.