Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006580788

FEI Number

3006580788

Entity Name

JAGO-PRO SP. Z O.O.

City/State/Country

JAWORZNO Slaskie, PL

Establishment Address

Szczakowska 35, JAWORZNO Slaskie 43-600, PL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Jago-Pro Sp. z o.o. (Owner Number: 10046017)

Owner / Operator Contact Address

Szczakowska 35, JAWORZNO, PL-24 43-600, PL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Brava Adhesive Remover Spray Brava Skin Barrier Spray mdoc topical hemostatic spray Curad QuickStop Bleeding Control Spray CVS Blood Stopping Spray Walgreens Blood Controlling Spray

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOX	Solvent, Adhesive Tape	General, Plastic Surgery	Class 1	878.4730	2014-01-24
EXB	Collector, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2014-01-24
QSY	Hemostatic Wound Dressing Without Thrombin Or Other Biologics	Unknown	Class U	N/A	2014-07-31

Official Correspondent

Beata Palka

US Agent Details

Mindy McCann Business: Qserve Group US Inc Email: USagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Jago-Pro Sp. z o.o.

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
K220566	Koag, LLC	Vascette HP (hemostatic pad)	2022-07-29
K080818	Hem Con Medical Technologies, Inc.	HEMCON BANDAGE, HEMCON BANDAGE OTC, HEMCON CHITOFLEX-SURGICAL DRESSING	2008-05-15
K893123	Les Laboratorires Brothier, S.A.	ADHESIVE BANDAGES & PADS FOR MINOR CUTS/SCRAPES	1990-02-13
K143462	Benq Materials Corporation	AnsCare ChitoClot Gauze (prescription use), AnsCare ChitoClot Gauze (over-the-counter use)	2015-05-08
K040208	Tz Medical, Inc.	NEPTUNE PAD, NEPTUNE DISC, NEPTUNE COMFORT-BAND, COMFORT-BAND	2004-05-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2012	Convatec Inc.	1	Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System (57 mm) Required for application to a patient immediately after ostomy surgery.

Similar Registrations

Registration Number	Establishment Name	Location
1811212	FERNDALE LABORATORIES, INC.	Ferndale, MI, US
3012910884	WALTERS HOUGHTON LTD.	Sandycroft, Deeside Flintshire, GB
3006789548	VALLEY PACKAGING INDUSTRIES, INC.	Appleton, WI, US
3012494290	SANICURE BV	SCHIPHOL Noord-Holland, NL
3042024535	PT YOUMI MEDIKA INDUSTRI	Batang Sulawesi Utara, ID

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006580788. Last updated year: 2026. Please use registration number 3006580788 when referencing this establishment in official correspondence.