| Primary Device ID | D79152210 |
| NIH Device Record Key | 2c9571c4-df54-4784-af29-77ef53061552 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Luminesse Clear PMMA Discs |
| Version Model Number | 5221 |
| Company DUNS | 094430642 |
| Company Name | TALLADIUM, INC. |
| 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 | 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 | D79152210 [Primary] |
| EBG | Crown And Bridge, Temporary, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-10-24 |
| D791CPMMAEX98300 | CPMMAEX9830 |
| D791CPMMAEX98250 | CPMMAEX9825 |
| D791CPMMAEX98210 | CPMMAEX9821 |
| D791CPMMAEX98200 | CPMMAEX9820 |
| D791CPMMAEX98100 | CPMMA-EX-98-10 |
| D79152290 | 5229 |
| D79152250 | 5225 |
| D79152240 | 5224 |
| D7915223Z0 | 5223Z |
| D79152230 | 5223 |
| D7915222Z0 | 5222Z |
| D79152220 | 5222 |
| D79152210 | 5221 |
| D79152200 | 5220 |
| D79152190 | 5219 |
| D79152180 | 5218 |
| D79152170 | 5217 |
| D7915216Z0 | 5216Z |
| D79152160 | 5216 |
| D7915215Z0 | 5215Z |
| D79152150 | 5215 |
| D7915214Z0 | 5214Z |
| D79152140 | 5214 |
| D7915213Z0 | 5213Z |
| D79152130 | 5213 |
| D7915212Z0 | 5212Z |
| D79152120 | 5212 |