Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Bioloren S.R.L. · 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) |
|---|---|---|---|---|---|
| K173643 | Trilor Disks, Blocks and Arches | Bioloren S.R.L. | 2018-02-24 | 89 | 0 |
| K121735 | FIBER DISK AND BLOCK PERMANENT, TRINIA | Bioloren S.R.L. | 2013-02-21 | 253 | 0 |
| K112186 | FIBER DISK AND BLOCK | Bioloren S.R.L. | 2011-11-08 | 102 | 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