TALON ACRYLICS, INC.

FDA Device Registration & Listing · Winchester, OR, US · Registration 3032727

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
3032727
FEI Number
3002717475
Entity Name
TALON ACRYLICS, INC.
City/State/Country
Winchester, OR, US
Establishment Address
710 Strauss Ave., Winchester, OR 97495, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device,Reprocess Single-Use Device
Owner / Operator
TALON ACRYLICS, INC. (Owner Number: 9037891)
Owner / Operator Contact Address
710 Strauss Ave., Winchester, OR 97495, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K071245
PMA Number
N/A

All Registered Proprietary Names

Talon & Revere Talon Thermoplastic Polymer/Revere Thermoplastic Polymer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2007-11-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TALON ACRYLICS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032727. Last updated year: 2026. Please use registration number 3032727 when referencing this establishment in official correspondence.
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