Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
ILE · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K830842 | OB HELP ARM | Lic-Orthion | 1983-04-05 | 19 | 0 |
| K823811 | OVERHEAD ARM SLINGS | Danek Medical, Inc. | 1983-01-14 | 28 | 0 |
| K823152 | OB HELP ARM | Orthion Corp. | 1982-11-05 | 16 | 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