Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Progressive Surgical Products, 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) |
|---|---|---|---|---|---|
| K982439 | PROXIDERM, MODELS TN 460, TN 90 460, BK 460 | Progressive Surgical Products, Inc. | 1998-09-08 | 56 | 0 |
| K970439 | PROXIDERM (D-460,D 90 460,D 180,460, PS 460) | Progressive Surgical Products, Inc. | 1997-04-16 | 70 | 0 |
| K942425 | PROXIDERM (TENTATIVE) | Progressive Surgical Products, Inc. | 1994-11-04 | 168 | 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