Regeneration Made Easy

Register below for access to trial product samples and a free ReGen Ready tee.

Meet Bionnovation

 Bionnovation has been developing regenerative materials since 1993. Today, as part of the Geistlich Group, we’re bringing that expertise directly to your general practice – with a streamlined portfolio, straightforward online ordering, and fast support designed around your workflow. 

A focused portfolio. Everything you need.

Ready-to-use. Small, precisely measured granules (0.25–1.0 mm) in four fill sizes — 0.5 cc, 1.0 cc, 2.0 cc, 4.0 cc — so there’s no chairside measuring or resizing.¹

How it’s made: A patented purification process that preserves natural bone architecture, strength, and porosity while fully deactivating organic residues.¹⁻⁴ Manufactured under ISO 13485, ISO 10993-1, and ISO 22442.²⁻⁴

Where it fits: Extraction socket preservation and minor ridge defects – the cases that show up in general practice every week, not the ones you’d refer out.

Thin, flexible, and tear-resistant.³ Adapts to defect sites without extra trimming or shaping.¹

How it’s made: Porcine collagen membrane manufactured to Geistlich quality standards — EC Full Quality Assurance System, MDSAP ISO 13485 certified.¹⁰,¹¹

Where it fits: Pairs with Oss XB for socket-site coverage and small-defect protection during healing.

A human-derived bone grafting option for practices that prefer allograft. Same focus on simplicity and clinical reliability.

How it’s made: Processed through an accredited US-based tissue bank to Geistlich Group quality standards.

Where it fits: The same everyday, general-practice cases as the rest of the portfolio — for the practices that reach for allograft instead.

Bionnovation is now available in the US. Qualifying practices can experience Bionnovation firsthand through our complimentary Trial Product Program *

  • A free product trial*
  • First access to on-demand educational content
  • Your ReGen Ready tee
  • Launch Updates and exclusive offers
  1. Instructions for Use, Bionnovation Oss XB, 2026
  2. Certificate Quality Management System, ISO 13485, Wishbone SA
  3. Biological Evaluation Report (BER), ISO 10993-1, Wishbone SA
  4. Animal tissues risk management & manufacturing controls, ISO 22442, Wishbone SA
  5. Data on File, Geistlich Pharma AG, Wolhusen, Switzerland (adhesion to curved surface, 200313560B033)
  6. Data on File, Geistlich Pharma AG, Wolhusen, Switzerland (mechanical properties, 160513560B053A)
  7. EC Certificate of Full Quality Assurance System
  8. MDSAP ISO 13485 Certificate

*The Trial Product Program is designed to help clinicians explore the Bionnovation portfolio through hands-on evaluation, supported by a dedicated Account Manager. Valid June 1–December 31, 2026. Each trial is limited to a total of 1 unit of biomaterial. Not applicable for Dental Service Organizations, Government, and Military Accounts. Submission and feedback form must be submitted and subject to qualification.