Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Biocore Medical Technologies, 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) |
|---|---|---|---|---|---|
| K022995 | COLLATEK HYDROGEL | Biocore Medical Technologies, Inc. | 2002-12-02 | 84 | 0 |
| K012995 | COLLATEK SHEET | Biocore Medical Technologies, Inc. | 2001-10-25 | 49 | 0 |
| K012997 | COLLATEK FOAM | Biocore Medical Technologies, Inc. | 2001-10-25 | 49 | 0 |
| K012990 | COLLATEK POWDER | Biocore Medical Technologies, Inc. | 2001-10-24 | 48 | 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