Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Millennium Medical Technologies, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
227 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K170449 | Autoclavable Suction Jar with Luer Lock extension - 250, 500 | Millennium Medical Technologies, Inc. | 2017-03-31 | 44 | 0 |
| K081039 | LIPO CANNULA | Millennium Medical Technologies, Inc. | 2008-07-10 | 90 | 0 |
| K031050 | PCW PERCUTANEOUS COMPRESSION WIRE | Millennium Medical Technologies, Inc. | 2003-07-14 | 103 | 0 |
| K020791 | HBS HEADLESS BONE SCREW | Millennium Medical Technologies, Inc. | 2002-06-06 | 87 | 0 |
| K012294 | WRISTORE FIXATOR | Millennium Medical Technologies, Inc. | 2002-03-04 | 227 | 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