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Biovision GmbH Entwicklung, Herstellung und Vertrieb von Biomaterialien

US

Last updated May 23, 2026

What Biovision GmbH Entwicklung, Herstellung und Vertrieb von Biomaterialien makes

Biovision GmbH develops and distributes synthetic bone graft materials designed for bone regeneration and reconstruction. Their portfolio includes resorbable biomaterials formulated to support tissue integration and structural support in orthopedic and maxillofacial applications.

The company’s products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. Biovision GmbH operates from the United States, adhering to regulatory requirements for synthetic bone graft materials.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
332192830

Catalogue (16)

DeviceModel / ReferenceRegistriesClassStatus
BioResorb® Macro Pore KE 19005510
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19014110
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010520
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010110
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010105
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010510
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19014120
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19005520
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19005110
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19005505
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19005120
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010120
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19002105
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19002505
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19010505
FDA UDI
Class IIActive
BioResorb® Macro Pore KE 19005105
FDA UDI
Class IIActive

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