Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dental Imaging Assoc., 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) |
|---|---|---|---|---|---|
| K902433 | DIA ANATOMIC ABUTMENT | Dental Imaging Assoc., Inc. | 1992-01-17 | 596 | 0 |
| K902434 | DIA HEALING CAP | Dental Imaging Assoc., Inc. | 1991-02-27 | 272 | 0 |
| K902435 | DIA IMPRESSION COPING | Dental Imaging Assoc., Inc. | 1991-02-20 | 265 | 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