Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014606366

FEI Number

3014606366

Entity Name

CAMARK SA

City/State/Country

Axioupoli Kentriki Makedonia, GR

Establishment Address

Industrial Park Axioupoli, Axioupoli Kentriki Makedonia 61400, GR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Camark (Owner Number: 10057719)

Owner / Operator Contact Address

1666 E Touhy Ave, Des Plaines, IL 60018, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NBY	Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene	General, Plastic Surgery	Class 2	878.5035	2018-05-17

Official Correspondent

No official correspondent registered.

US Agent Details

Stephanie Wasielewski Business: Hu-Friedy Mfg Co LLC Email: swasielewski@hu-friedy.com Phone: (847) 2574500

Related Public Records

Same Entity

Camark

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014606366. Last updated year: 2026. Please use registration number 3014606366 when referencing this establishment in official correspondence.