| Primary Device ID | D7915212Z0 | 
| NIH Device Record Key | 80887480-9efb-4139-9d80-f6c6d6c40284 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Luminesse Clear PMMA Discs | 
| Version Model Number | 5212Z | 
| 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 | D7915212Z0 [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 |