GARRECO, LLC

FDA Device Registration & Listing · Heber Springs, AR, US · Registration 3009426332

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
3009426332
FEI Number
3009426332
Entity Name
GARRECO, LLC
City/State/Country
Heber Springs, AR, US
Establishment Address
430 Hiram Road, Heber Springs, AR 72543, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Garreco, LLC. (Owner Number: 10042968)
Owner / Operator Contact Address
430 Hiram Road, Heber Springs, AR 72543, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K910676
PMA Number
N/A

All Registered Proprietary Names

PEMACO BITE BLOCK RODS-MEDIUM SOFT & MEDIUM HARD PEMACO ECONOMY BASE PLATE WAX-MEDIUM SOFT Garreco Base Plate Wax Sheets All Season Garreco Base Plate Wax Sheets Medium Soft PEMACO 3000 INTRAORAL DENTAL WAX PEMACO ECONOMY BASE PLATE WAX-MEDIUM HARD Garreco Base Plate Wax Sheets Medium Hard Garreco PEMACO INTRAORAL DENTAL WAX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2018-11-01
EBH Material, Impression Tray, Resin Dental Class 1 872.3670 2013-01-15
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2018-11-01
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2018-11-01
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2018-11-01
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2016-02-11
EJL Bur, Dental Dental Class 1 872.3240 2013-01-15
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2016-02-11
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2018-11-01

Official Correspondent

Kristofer Mainar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Garreco, LLC.
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 3009426332. Last updated year: 2026. Please use registration number 3009426332 when referencing this establishment in official correspondence.
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