Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sedatelec — 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) |
|---|---|---|---|---|---|
| K101267 | PREMIO 10 MOXA | Sedatelec | 2010-12-03 | 212 | 0 |
| K060392 | ASP TITANIUM | Sedatelec | 2006-04-26 | 70 | 0 |
| K983798 | SEDATELEC ASP ACUPUNCTURE NEEDLES | Sedatelec | 1999-08-27 | 303 | 0 |
| K983800 | DN ACUPUNTURE NEEDLES | Sedatelec | 1999-08-27 | 303 | 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