Dri Mark Products, Inc.

FDA Device Registration & Listing · Bethpage, NY, US · Registration 2436880

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
2436880
FEI Number
1000204659
Entity Name
Dri Mark Products, Inc.
City/State/Country
Bethpage, NY, US
Establishment Address
999 S Oyster Bay Rd, Suite 312, Bethpage, NY 11714, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dri Mark Products Inc. (Owner Number: 10042284)
Owner / Operator Contact Address
999 S. Oyster Bay Road, Suite 312, Bethpage, NY 11714, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dri Mark Surgical Skin Marker arker

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FZZ Marker, Skin General, Plastic Surgery Class 1 878.4660 2012-11-08

Official Correspondent

Cathy Owen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dri Mark Products Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2436880. Last updated year: 2026. Please use registration number 2436880 when referencing this establishment in official correspondence.
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