Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rimed , Ltd. — 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) |
|---|---|---|---|---|---|
| K143476 | Digi-One | Rimed , Ltd. | 2015-06-23 | 200 | 0 |
| K062578 | DIGI-LITE TCD DEVICE | Rimed , Ltd. | 2006-09-18 | 18 | 0 |
| K974588 | INTRA-VIEW BILATERAL TRANSCRANIAL DOPPLER DEVICE, SMART-LITE | Rimed , Ltd. | 1998-08-07 | 241 | 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