Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Intermedic Arfran, SA · 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) |
|---|---|---|---|---|---|
| K091323 | MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST | Intermedic Arfran, SA | 2009-06-04 | 30 | 0 |
| K053540 | INTERMEDIC DIODE LASER FAMILY 810NM AND 980NM (AND THE DELIV | Intermedic Arfran, SA | 2006-09-06 | 260 | 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