SEYITLER KIMYA SANAYI A.S.

FDA Device Registration & Listing · Manisa, TR · Registration 3025771275

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
3025771275
FEI Number
3025771275
Entity Name
SEYITLER KIMYA SANAYI A.S.
City/State/Country
Manisa, TR
Establishment Address
1. Osb 2007 Street No:5-7 Turgutlu/Manisa Turkey, Manisa TR-45400, TR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Seyitler Kimya Sanayi A.S. (Owner Number: 10087005)
Owner / Operator Contact Address
1. Osb 2007 Street No:5-7 Turgutlu/Manisa Turkey, Manisa, TR-45 TR-45400, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Novapore Paper Plaster;Novafix Elastic Plaster Nova Aid Plaster; Novaplast Fabric Plaster; Novasilk Silk Plaster; Novatrans Transparent Plaster Maxipore IV Dress; Maxipore PU IV, Maxipore PU ROLL Novaband First Aid Plaster;Pelikan First Aid Plaster Nova Compress Kurtplast Perforated Plaster; Maxistrip Dermapore Paper Plaster, Enjeksiyon Plaster, Nova Dialysis, Topplast Kurtplast First Aid Plaster ; Dermafix Transparent Plaster Maxipore Dress Wound Pad;Maxipore Dress PU Wound Pad; Maxipore Pu Film Unipore Elastic Plaster; Medibez Fabric Plaster; Mediipek Silk Plaster Nova Corn Plaster NOVAFIX HYPOALLERGENIC SURGICAL TAPE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2022-12-30

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Seyitler Kimya Sanayi A.S.
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025771275. Last updated year: 2026. Please use registration number 3025771275 when referencing this establishment in official correspondence.
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