# K072402: Flex-Star V

- Pathway: 510(k) (Traditional)
- Applicant: Cmp Industries, LLC
- Decided: Oct 19, 2007 after 53 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K250617: Apex Flex (2025), 3 descendants of its own
- K261626: UltraPrint Flexible Denture UV (2026), 0 descendants of its own
- K261474: DENTCA Tru Flexible (2026), 0 descendants of its own
- K253365: LuxCreo Flexible Partial Denture Resin (2025), 0 descendants of its own
- K170375: Nobilplast Denture Resin (2017), 0 descendants of its own

## Indications for use
CMP's Flex-Star V is used for the fabrication of partial or full removable dentures, as well as occusal splints and night guards. It is to be used only by professional dental practitioners who make or repair dentures for patients

Source page: https://510kreport.com/device/K072402
Methodology: https://510kreport.com/methodology