Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Inter-Med/Vista Dental Products · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
148 daysmedian FDA review time
324 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K193357 | V-Mix | Inter-Med/Vista Dental Products | 2020-10-23 | 324 | 0 |
| K193409 | Vista Rinse, Vista Rinse Plus | Inter-Med/Vista Dental Products | 2020-09-09 | 275 | 0 |
| K193447 | Vista Dyes | Inter-Med/Vista Dental Products | 2020-03-11 | 89 | 0 |
| K193389 | Vista Clear | Inter-Med/Vista Dental Products | 2020-03-04 | 89 | 0 |
| K190220 | Vista FS, Vista FS Liquid | Inter-Med/Vista Dental Products | 2019-06-10 | 125 | 1 |
| K170101 | Valiant Curing Light | Inter-Med/Vista Dental Products | 2017-06-08 | 148 | 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