Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ge Lunar Corp. — 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) |
|---|---|---|---|---|---|
| K030962 | DPX SERIES BRAVO DUO BONE DENSITOMETER | Ge Lunar Corp. | 2003-07-25 | 120 | 0 |
| K023554 | DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWARE | Ge Lunar Corp. | 2002-12-20 | 58 | 0 |
| K011917 | ADVANCED HIP ASSESSMENT SOFTWARE | Ge Lunar Corp. | 2001-08-03 | 44 | 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