Dedeco International, Inc.

FDA Device Registration & Listing · LONG EDDY, NY, US · Registration 1316367

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
1316367
FEI Number
1316367
Entity Name
Dedeco International, Inc.
City/State/Country
LONG EDDY, NY, US
Establishment Address
11617 State Route 97, LONG EDDY, NY 12760, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dedeco International, Inc. (Owner Number: 1316367)
Owner / Operator Contact Address
11617 State Route 97, Long Eddy, NY 12760, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bur, Dental Instrument Diamond Dental Point Abrasive Floss Dental Point Abrasive Agent, Polishing, Abrasive, Oral Cavity

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJL Bur, Dental Dental Class 1 872.3240 2001-12-05
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 2001-12-05
JES Floss, Dental Dental Class 1 872.6390 2020-01-10
EHL Point, Abrasive Dental Class 1 872.6010 2001-12-05
EJR Agent, Polishing, Abrasive, Oral Cavity Dental Class 1 872.6030 2001-12-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dedeco International, 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
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10
K121698 Dentsply International, Inc. NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN 2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1316367. Last updated year: 2026. Please use registration number 1316367 when referencing this establishment in official correspondence.
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