# K231072: Anthogyr FlexiBase® titanium bases for Axiom® BL

- Pathway: 510(k) (Traditional)
- Applicant: Anthogyr
- Decided: Jan 4, 2024 after 265 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K894844 (1990). 171 ancestors in all.
No later device cites it as a predicate yet.
0 of 172 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150203: Medentika CAD/CAM Abutments, Medentika GmbH (2015) Summary page 6.

## Indications for use
Anthogyr FlexiBase® titanium bases for Axiom® BL are indicated for use as a support for single-unit customized prosthetic restorations. All digitally designed copings and / or crowns for use with the Anthogyr Flexibase® titanium bases for Axiom® BL are intended to be sent to Straumann for manufacturing by a validated milling center (Straumann CARES System).

Source page: https://510kreport.com/device/K231072
Methodology: https://510kreport.com/methodology