KURTSAN PHARMACEUTICALS, INC.

FDA Device Registration & Listing · Bandirma Balikesir, TR · Registration 3004651943

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
3004651943
FEI Number
3004651943
Entity Name
KURTSAN PHARMACEUTICALS, INC.
City/State/Country
Bandirma Balikesir, TR
Establishment Address
Akcapinar Mahallesi, Akcapinar Sokak No. 266, [Previously called: Balikesir Yolu 10 km], Bandirma Balikesir 10200, TR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kurtsan Pharmaceuticals, Inc. (Owner Number: 10024944)
Owner / Operator Contact Address
Istoc Otomarket A-2, Blok Burak Plaza K.7 Bagcilar, Istanbul, TR-34 34218, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PLASTER PLUS AQUA PLASTER PLUS (Regular ; Kids ; Aloe Vera ; Shave ; Mix ; Antibacterial ; Haemostatic ; Aqua ; Flex) PLASTER PLUS FLEX CORN PLASTER CORN SALICYLIC ACETIC REMOVAL PLASTER DRAGON PLASTER ROLL YAKI PLASTER COLD & WARM PLASTER CAPSICUM PLASTER CORN REMOVAL PLASTER YABELET PLUS YABELET PLUS BIG DRAGON PLASTER FORTE

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 2008-08-25
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2008-03-04

Official Correspondent

No official correspondent registered.

US Agent Details

Danny Rosenbaum Business: Danny D. Rosenbaum Email: danny.rosenbaum.rp@gmail.com Phone: (973) 9377675

Related Public Records

Same Entity

Kurtsan Pharmaceuticals, 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
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 3004651943. Last updated year: 2026. Please use registration number 3004651943 when referencing this establishment in official correspondence.
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