Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Pillar Surgical, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
143 daysmedian FDA review time
143 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K002633 | SILMAX PECTORAL IMPLANT | Pillar Surgical, Inc. | 2000-11-21 | 90 | 0 |
| K002629 | SILMAX CONTOUR CARVING BLOCK IMPLANT | Pillar Surgical, Inc. | 2000-11-20 | 89 | 0 |
| K992242 | PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS | Pillar Surgical, Inc. | 1999-11-22 | 143 | 0 |
| K992240 | PILLAR MALAR IMPLANT | Pillar Surgical, Inc. | 1999-11-22 | 143 | 0 |
| K992239 | PILLAR CHIN IMPLANT | Pillar Surgical, Inc. | 1999-11-22 | 143 | 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