Bredent GmbH & Co. KG · Class II · Cleared Sep 14, 2010
| K-number | K101064 |
| Device name | BREDENT NOVO.LIGN A/ BREDENT NOVO.LIGN P |
| Applicant | Bredent GmbH & Co. KG |
| Product code | ELM |
| Device class | Class II |
| Decision date | Sep 14, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 872.3590 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov