Facility

PREMIER DENTAL PRODUCTS CO.

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	2511556
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	1710 Romano Dr PLYMOUTH MEETING, PA, US 19462
Registration status	Active · expires 2026
Parent company	Premier Dental Products Company (owner-operator 2511556)
Brand names	Premier IntegraBond

Activity by year

Recalls (1)

Devices registered here (1)

Material, Tooth Shade, Resin
Product code EBF (opens in a new tab) · Class II · Dental · 21 CFR 872.3690

Recalls & enforcement

Class IIOngoing2025-02-27
The hardness not meeting the material specification and may cause the diamond bur to bend.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “PREMIER DENTAL PRODUCTS CO. (FEI 2511556) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2511556-premier-dental-products-co/

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