The following data is part of a premarket notification filed by Cmp Industries Llc. with the FDA for Flex-star V.
| Device ID | K072402 |
| 510k Number | K072402 |
| Device Name: | FLEX-STAR V |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | CMP INDUSTRIES LLC. 413 NORTH PEARL ST. Albany, NY 12207 |
| Contact | Devon O Howe |
| Correspondent | Devon O Howe CMP INDUSTRIES LLC. 413 NORTH PEARL ST. Albany, NY 12207 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-27 |
| Decision Date | 2007-10-19 |