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Data / Medical devices / United States / Talon Acrylics, Inc.

Talon Acrylics, Inc.: FDA-registered device maker in Winchester, OR, United States, 1 510(k) clearance

Talon Acrylics, Inc. is registered with the FDA (registration 3032727) in Winchester, OR, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 2, 2007. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3032727
FEI number
3002717475
Address
710 Strauss Ave., Winchester, OR, United States, 97495
Owner or operator
TALON ACRYLICS, INC. (9037891)
Roles
Manufacturer, Repackager or relabeler, Reprocessor
First device listed
November 30, 2007
Registered through
2026
Brand names listed
Talon & Revere, Talon Thermoplastic Polymer/Revere Thermoplastic Polymer

Devices it lists

DeviceProduct codeClassRoleSource
Resin, Denture, Relining, Repairing, RebasingEBI2Manufacturer, Repackager or relabeler, Reprocessoraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 2, 2007K071245TALON AND REVEREEBISubstantially EquivalentTalon Acrylics, Inc.accessdata.fda.gov

Compare with other makers

Updated August 2, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.