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
- 2,897
- Deaths
- 0
- Injuries
- 2,897
- Malfunctions
- 0
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.
Monitor Anthogyr automatically
DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.