Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dvo Extremity Solutions, LLC — 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) |
|---|---|---|---|---|---|
| K073331 | DVO EXTENDED ARTICULATION HUMERAL HEADS | Dvo Extremity Solutions, LLC | 2008-02-19 | 84 | 0 |
| K060988 | TOTAL AND HEMI SHOULDER SYSTEM | Dvo Extremity Solutions, LLC | 2006-12-06 | 240 | 13 |
| K052754 | WRIST FUSION PLATE | Dvo Extremity Solutions, LLC | 2005-10-27 | 27 | 0 |
| K052150 | VOLAR PLATE SYSTEM | Dvo Extremity Solutions, LLC | 2005-09-08 | 31 | 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