CROWN DELTA CORP.

FDA Device Registration & Listing · Yorktown, NY, US · Registration 2431069

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
2431069
FEI Number
2431069
Entity Name
CROWN DELTA CORP.
City/State/Country
Yorktown, NY, US
Establishment Address
1520 FRONT ST., Yorktown, NY 10598, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
CROWN DELTA CORP. (Owner Number: 2431069)
Owner / Operator Contact Address
1520 FRONT ST., --, Yorktown Hgts, NY 10598, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Podiatric Impression Material Vinyl Silicone Material Silicone Elastomer Putty VPS Silicone Adhesive Impression Material Syringe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ELW Material, Impression Dental Class 2 872.3660 2008-07-07
MNE Orthosis, Moldable, Supportive, Skin Protective Physical Medicine Class 1 890.3475 2007-11-28
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2008-07-03
ELW Material, Impression Dental Class 2 872.3660 2008-07-03
ELW Material, Impression Dental Class 2 872.3660 2016-06-16
MVL Cord, Retraction Unknown Class U N/A 2016-06-16
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2008-07-03
ELW Material, Impression Dental Class 2 872.3660 2014-01-24
EID Syringe, Restorative And Impression Material Dental Class 1 872.4565 2010-04-16

Official Correspondent

MARK KONOPKA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CROWN DELTA CORP.
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
K952614 Dentsply Intl. JELTRATE PLUS ANTIMICROBIAL IMPR. MATERIAL 1996-08-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2431069. Last updated year: 2026. Please use registration number 2431069 when referencing this establishment in official correspondence.
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