Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ri Mos. S.R.L. — 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) |
|---|---|---|---|---|---|
| K992926 | GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195) | Ri Mos. S.R.L. | 1999-10-26 | 56 | 0 |
| K991895 | RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) | Ri Mos. S.R.L. | 1999-08-12 | 70 | 0 |
| K991827 | GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS | Ri Mos. S.R.L. | 1999-07-19 | 52 | 0 |
| K983897 | CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE | Ri Mos. S.R.L. | 1999-02-01 | 90 | 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