Bonegraft Biomaterials Co. - Manufacturer Profile

Explore comprehensive manufacturer profile for Bonegraft Biomaterials Co. through Pure Global AI's free EU medical device database. This company manufactures 5630 medical devices registered with EUDAMED across 3 risk classes based in Turkey.

This page provides detailed insights including recent registrations, risk class distribution (Class III: 5320, Class IIb: 156, Class IIa: 154), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.

Free Manufacturer Profile

5630 Devices

3 Risk Classes

Bonegraft Biomaterials Co.

Manufacturer - Turkey

5630

Total Devices

Risk Classes

2022

Earliest Version

DJ Fang

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Recent Products (Latest 10)

Most recently updated devices in the database

Device Name	Risk Class	Detail
Bonegraft Bone Cement Bone Drill	Class IIa
Biongraft Bone Cement Applicator Guide Wire (Kirschner wire)	Class IIa
Kaulmed Vertebroplasty, Percutaneous Posterior, Vertebroplasty Bone Interference Set, Metal-Plastic	Class IIa
Spineorth Bone Cement Applicator Guide Cannula	Class IIa
Bonegraft Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit (2pcs Filler+ 2 pcs Pusher)	Class IIa
Powerbone Bone Filler and Pusher For Cannulated Screw (Short)	Class IIa
Powerbone Bone Cement Applicator Guide Wire (Kirschner wire)	Class IIa
Ecobone Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit	Class IIa
Powerbone Bone Cement Bone Drill	Class IIa
Biongraft Bone Filler and Pusher For Cannulated Screw(Short)	Class IIa

Risk Class Distribution

Breakdown by risk classification

Class III

5320(94.5%)

Class IIb

156(2.8%)

Class IIa

154(2.7%)