Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
M. D. Products — 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) |
|---|---|---|---|---|---|
| K902948 | COMFORTRON II (TENS) | M. D. Products | 1990-12-17 | 165 | 0 |
| K884586 | COMFORTRON DENTAL ANESTHESIA APPARATUS | M. D. Products | 1989-04-14 | 163 | 0 |
| K871227 | LES RAD FILTER | M. D. Products | 1987-06-29 | 94 | 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