Facility

Danville Materials Research Center

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

Key facts

2recalls · 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)	3010664129
Establishment type	Manufacture Medical Device
Location	4020 E Leaverton Ct Anaheim, CA, US 92807
Registration status	Active · expires 2026
Parent company	Zest Anchors, LLC (owner-operator 2023950)

Activity by year

Recalls (2)

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 IIOngoing2019-11-22
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
Class IITerminated2014-01-16
Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR® Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently noted by Zest that in order to provide an …

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. “Danville Materials Research Center (FEI 3010664129) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3010664129-danville-materials-research-center/

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