Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Goldsmith & Revere, Inc. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K951865 | ULTRA SPHERICAL AMALGAM ALLOY | Goldsmith & Revere, Inc. | 1995-05-25 | 34 | 0 |
| K933309 | PRINCE | Goldsmith & Revere, Inc. | 1993-10-01 | 86 | 0 |
| K821222 | GOLDSMITH & REVERE TENARY ALLOY | Goldsmith & Revere, Inc. | 1982-05-24 | 27 | 0 |
| K820617 | DISPERSED PHASE ALLOY | Goldsmith & Revere, Inc. | 1982-03-25 | 17 | 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