Manufacturer profile

Bonegraft Biomaterials Co.

EU EUDAMEDTurkey5630 registered devices

VerifiedEUDAMED · official EU database

5,630

Total devices

Risk classes

2022

Earliest version

2024

Latest version

Regulatory footprint

Search Bonegraft Biomaterials Co. across other regulatory registries

Recent products (latest 10)

Most recently updated devices in the database

Bonegraft Bone Cement Bone Drill

08681781334274

Class IIa

Biongraft Bone Cement Applicator Guide Wire (Kirschner wire)

08681781334472

Class IIa

Kaulmed Vertebroplasty, Percutaneous Posterior, Vertebroplasty Bone Interference Set, Metal-Plastic

08681781335349

Class IIa

Spineorth Bone Cement Applicator Guide Cannula

08681781350014

Class IIa

Bonegraft Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit (2pcs Filler+ 2 pcs Pusher)

08681781334311

Class IIa

Powerbone Bone Filler and Pusher For Cannulated Screw (Short)

08681781334229

Class IIa

Powerbone Bone Cement Applicator Guide Wire (Kirschner wire)

08681781334113

Class IIa

Ecobone Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit

08681781334427

Class IIa

Powerbone Bone Cement Bone Drill

08681781334151

Class IIa

Biongraft Bone Filler and Pusher For Cannulated Screw(Short)

08681781334588

Class IIa

Risk class distribution

Breakdown by risk classification

Class III532094.5% of total

Class IIb1562.8% of total

Class IIa1542.7% of total

About this 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.