ESSTECH, INC

FDA Device Registration & Listing · Essington, PA, US · Registration 3008569063

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
3008569063
FEI Number
3008569063
Entity Name
ESSTECH, INC
City/State/Country
Essington, PA, US
Establishment Address
48 W Powhattan Ave, Essington, PA 19029, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Esstech, Inc (Owner Number: 10093824)
Owner / Operator Contact Address
48 Powhattan Ave., Essington, PA 19029, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FP3D

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 2025-07-26

Official Correspondent

Thomas Barclift

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Esstech, 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 3008569063. Last updated year: 2026. Please use registration number 3008569063 when referencing this establishment in official correspondence.
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