Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Dental Ventures of America, Inc. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K000894 | C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL | Dental Ventures of America, Inc. | 2000-05-19 | 60 | 0 |
| K842377 | MS NONPRECIOUS CROWN & BRIDGE ALLOY | Dental Ventures of America, Inc. | 1984-07-31 | 43 | 0 |
| K780808 | PIEZOMATIC ULTRASONIC SCALER (SYSTEM S) | Dental Ventures of America, Inc. | 1978-06-22 | 35 | 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