ET Rigid AbutmentRecalls & reported problems across all models
Hiossen, Inc. · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one ET Rigid Abutment model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 4
We found 4 models of ET Rigid Abutment by Hiossen, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
4 FDA recall records name at least one of these models by its device identifier, 4 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
ET Rigid Abutment recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jan 27, 2025Open, Classified
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
Z-1275-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Jan 27, 2025Open, Classified
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
Z-1273-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Jan 27, 2025Open, Classified
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
Z-1272-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Jan 27, 2025Open, Classified
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
Z-1271-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
ET Rigid Abutment models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ET Rigid Abutment ETRGA4524MPAbutment, Implant, Dental, Endosseous1 recall0 reports
- ET Rigid Abutment ETRGA4544MPAbutment, Implant, Dental, Endosseous1 recall0 reports
- ET Rigid Abutment ETRGA4515MPAbutment, Implant, Dental, Endosseous1 recall0 reports
- ET Rigid Abutment ETRGA4537MPAbutment, Implant, Dental, Endosseous1 recall0 reports
Other Hiossen, Inc. products
All Hiossen, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page