Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Orthogem Limited — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K110787 | TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15) | Orthogem Limited | 2011-04-21 | 31 | 0 |
| K070132 | TRIPORE, MODELS HA, BP90, BP15 | Orthogem Limited | 2007-07-13 | 178 | 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