| Primary Device ID | D96710016 |
| NIH Device Record Key | 39d6e2de-816b-49a4-a5d0-e01e5a0b59ad |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Renew MDP |
| Version Model Number | Regular Pack |
| Catalog Number | 10016 |
| Company DUNS | 859546940 |
| Company Name | PREVEST DENPRO LIMITED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D96710016 [Primary] |
| KLE | Agent, Tooth Bonding, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-01 |
| Device Publish Date | 2024-04-23 |
| D967200270 - Fusion Core DC Flo and Fusion Bond DC | 2025-02-18 |
| D96710001 - Fusion Bond 7 | 2024-05-01 |
| D96710002 - Fusion Bond 7 | 2024-05-01 |
| D96710003 - Fusion Bond 5 | 2024-05-01 |
| D96710004 - Fusion Bond 5 | 2024-05-01 |
| D96710005 - Fusion Bond DC | 2024-05-01 |
| D96710016 - Renew MDP | 2024-05-01 |
| D96710016 - Renew MDP | 2024-05-01 |
| D96710017 - Renew Universal | 2024-05-01 |