Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Sainath Intellectual Properties, LLC · 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) |
|---|---|---|---|---|---|
| K102572 | IYUNNI 3ID SUPRAPUBIC CYSTOSTOMY TUBE KIT | Sainath Intellectual Properties, LLC | 2010-12-27 | 110 | 0 |
| K100173 | IYUNNI 3ID TRI-FUNNEL FEEDING TUBE KIT | Sainath Intellectual Properties, LLC | 2010-04-16 | 85 | 0 |
| K092049 | IYUNNI 3ID TRI-FUNNEL GASTROSTOMY TUBE KIT | Sainath Intellectual Properties, LLC | 2009-10-09 | 94 | 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