Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Bio-Dyne, 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) |
|---|---|---|---|---|---|
| K900691 | BIODYNE INSTRUMENT WIPES | Bio-Dyne, Inc. | 1990-03-08 | 23 | 0 |
| K883984 | HEMORX COLD PACK | Bio-Dyne, Inc. | 1988-12-22 | 93 | 0 |
| K864261 | MODEL 3500 INFANT RESPIRATION & HEART RATE MONITOR | Bio-Dyne, Inc. | 1987-03-27 | 149 | 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