| Primary Device ID | D9491120410 |
| NIH Device Record Key | 0c4dd9a5-ffab-4b88-bae0-ae441e8f31ff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bioclear Diamond Wedge |
| Version Model Number | Extra Large |
| Company DUNS | 059020838 |
| Company Name | Bioclear Matrix Systems |
| Device Count | 50 |
| 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 | D9491120410 [Unit of Use] |
| HIBCC | D949112041041 [Primary] |
| HIBCC | D949112041081 [Primary] |
| HIBCC | D949112041101 [Primary] |
| HIBCC | D949112041161 [Primary] |
| HIBCC | D949112041500BG1 [Primary] |
| HIBCC | D949112041501 [Primary] |
| HIBCC | D949112041503 [Primary] |
| HIBCC | D94911204150BG1 [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 | 2023-08-15 |
| Device Publish Date | 2023-08-07 |
| 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. |