Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sage In-Vitro Fertilization, Inc. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K073522 | VITRIFICATION KIT & VITRIFICATION WARMING KIT | Sage In-Vitro Fertilization, Inc. | 2008-10-10 | 301 | 0 |
| K053646 | INVITRO MATURATION MEDIA | Sage In-Vitro Fertilization, Inc. | 2006-07-14 | 196 | 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