| Primary Device ID | D9491120110 |
| NIH Device Record Key | 52b4287d-c2ff-483e-8b24-9a4837b7f595 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bioclear Diamond Wedge |
| Version Model Number | Small |
| Company DUNS | 059020838 |
| Company Name | Bioclear Matrix Systems |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D9491120110 [Primary] |
| HIBCC | D949112011021 [Primary] |
| HIBCC | D949112011041 [Primary] |
| HIBCC | D949112011081 [Primary] |
| HIBCC | D949112011101 [Primary] |
| HIBCC | D949112011161 [Primary] |
| HIBCC | D949112011500BG1 [Primary] |
| HIBCC | D949112011503 [Primary] |
| HIBCC | D94911201150BG1 [Primary] |
| EJB | Handle, Instrument, Dental |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-18 |
| Device Publish Date | 2023-09-10 |
| D9491120510 | Plastic wedge used in dental restorations. |
| D9491120410 | Plastic wedge used in dental restorations. |
| D9491120310 | Plastic wedge used in dental restorations. |
| D9491120210 | Plastic wedge used in dental restorations. |
| D949112011501 | Plastic wedge used in dental restorations. |
| D9491120110 | Plastic wedge used in dental restorations. |