Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Cmp Industries, LLC — Predicate Candidate Screening
7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
254 days90th percentile
7clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K170423 | DentureID Microchip | Cmp Industries, LLC | 2017-10-25 | 254 | 0 |
| K170375 | Nobilplast Denture Resin | Cmp Industries, LLC | 2017-10-02 | 237 | 0 |
| K072851 | POLYSTAR 79 DENTURE BASE RESIN | Cmp Industries, LLC | 2008-02-20 | 139 | 0 |
| K072402 | FLEX-STAR V | Cmp Industries, LLC | 2007-10-19 | 53 | 0 |
| K033020 | IMPAK ACRYLIC REPAIR RESIN LIQUID | Cmp Industries, LLC | 2003-12-19 | 84 | 2 |
| K953594 | VULCAN | Cmp Industries, LLC | 1995-09-05 | 36 | 0 |
| K902972 | FLEXOR (DENTURE ACRYLIC RELINE MATERIAL) | Cmp Industries, LLC | 1990-10-04 | 90 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda