Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dgimed Ortho, Inc. · 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) |
|---|---|---|---|---|---|
| K132830 | DISTALOCK TIBIAL IM NAIL SYSTEM | Dgimed Ortho, Inc. | 2014-01-06 | 118 | 0 |
| K100312 | DISTALOCK FEMORAL INTRAMEDULLARY NAIL SYSTEM | Dgimed Ortho, Inc. | 2010-04-20 | 75 | 0 |
| K091309 | REVOLUTION FEMORAL INTRAMEDULLARY NAIL SYSTEM, MODEL DGOOXX | Dgimed Ortho, Inc. | 2009-11-05 | 185 | 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