Anthogyr
FDA adverse event reports naming Anthogyr as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ANTHOGYR.
- Total reports
- 60,399
- Deaths
- 0
- Injuries
- 58,010
- Malfunctions
- 2,389
Reports per year
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- 2016-09-08TerminatedDevice Design
Axiom REG 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.
Following a FDA inspection showing that the firm failed to validate the design and process of its implants.
- 2016-09-08TerminatedDevice Design
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.
Following a FDA inspection showing that the firm failed to validate the design and process of its implants.
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