Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Axiom 2.8 implants Sterile The Axiom REG implants are used Recalled by Anthogyr Due to Following a FDA inspection showing that the firm...

Date: June 20, 2016
Company: Anthogyr
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Anthogyr directly.

Affected Products

Axiom 2.8 implants Sterile The Axiom REG implants are used as artificial root structures for replacement of missing teeth. They can be used for stabilization of removable prostheses or fixation of single tooth restorations or partial dentures. There are different diameters and different lengths for each diameter.

Quantity: 10 units

Why Was This Recalled?

Following a FDA inspection showing that the firm failed to validate the design and process of its implants.

Where Was This Sold?

This product was distributed to 3 states: NY, NC, OR

Affected (3 states)Not affected

About Anthogyr

Anthogyr has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report