Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Reliance Medical Systems — 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) |
|---|---|---|---|---|---|
| K181118 | Reliance Lumbar IBF System | Reliance Medical Systems | 2019-01-09 | 257 | 0 |
| K180687 | Reliance Lumber IBF System | Reliance Medical Systems | 2018-05-15 | 61 | 0 |
| K101112 | RELIANCE SPINAL SCREW SYSTEM | Reliance Medical Systems | 2010-11-04 | 197 | 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