| Primary Device ID | 00863995000123 |
| NIH Device Record Key | 888afba0-95b3-4efd-bc59-1ce69ca883af |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DenSureFit |
| Version Model Number | DSFUPPER |
| Company DUNS | 080416887 |
| Company Name | OTC DENTAL CORPORATION |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00863995000123 [Primary] |
| EBI | Resin, Denture, Relining, Repairing, Rebasing |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-06 |
| Device Publish Date | 2026-02-26 |
| 00863995000109 | DenSureFit is an over-the-counter soft reline kit. It consists of 2 applicators of vinyl polysil |
| 00863995000123 | DenSureFit is an over-the-counter soft reline kit. It consists of 2 applicators of vinyl polysil |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DENSUREFIT 86705481 5291548 Live/Registered |
OTC Dental 2015-07-27 |