The following data is part of a premarket notification filed by Quest Dental Usa Corp. with the FDA for Pure Pmma Disc.
Device ID | K172281 |
510k Number | K172281 |
Device Name: | PuRE PMMA Disc |
Classification | Crown And Bridge, Temporary, Resin |
Applicant | Quest Dental USA Corp. 17865 Sky Park Circle Suite L1 Irvine, CA 92614 |
Contact | Hirotaka Mori |
Correspondent | Takahiro Haruyama Globizz Corporation 1411 W 190th St Gardena, CA 90248 |
Product Code | EBG |
CFR Regulation Number | 872.3770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-28 |
Decision Date | 2017-10-19 |
Summary: | summary |