Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment— 510(k) K241722
Substantially EquivalentElos Medtech Pinol A/S
FDA 510(k) clearance K241722 for Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment, Substantially Equivalent on 2024-09-13. Applicant: Elos Medtech Pinol A/S.
Clearance details
- Applicant
- Elos Medtech Pinol A/S
- Product code
- Code NHA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Goerloese, DK
Adverse events under product code NHA
product code NHA- Injury
- 1,270
- Malfunction
- 2,860
- Total
- 4,130
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.