Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010413864

FEI Number

3010413864

Entity Name

Nolato Stargard Sp. z o.o.

City/State/Country

Stargard Zachodniopomorskie, PL

Establishment Address

Uslugowa 1, Stargard Zachodniopomorskie 73-110, PL

Establishment Type(s)

Sterilize Medical Device for Another Party (Contract Sterilizer),Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Nolato Stargard Sp. z o.o. (Owner Number: 10044127)

Owner / Operator Contact Address

Uslugowa 1, Stargard, PL-32 73-110, PL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CERAMENT G NidOil

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QRR	Filler, Bone Void, Calcium Compound Containing Single Approved Aminoglycoside	Orthopedic	Class 2	888.3046	2022-06-15
MQL	Media, Reproductive	Obstetrics/Gynecology	Class 2	884.6180	2024-04-18

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Nolato Stargard 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
K011481	Conception Technologies	10% PVP; 10% PVP IN EBSS SOLUTION	2001-07-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010413864. Last updated year: 2026. Please use registration number 3010413864 when referencing this establishment in official correspondence.