The following data is part of a premarket notification filed by Belport Co., Inc. with the FDA for Gingi-plain Cords & Braids.
| Device ID | K812120 |
| 510k Number | K812120 |
| Device Name: | GINGI-PLAIN CORDS & BRAIDS |
| Classification | Floss, Dental |
| Applicant | BELPORT CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JES |
| CFR Regulation Number | 872.6390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-07-27 |
| Decision Date | 1981-09-08 |