Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medical Technology Development Corp. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
38 daysmedian FDA review time
247 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K941488 | DEVMED DOUBLE-BALLOON UROLOGICAL CATHETER | Medical Technology Development Corp. | 1994-11-30 | 247 | 0 |
| K862315 | FYODOROV COLLAGEN CORNEAL SHIELD | Medical Technology Development Corp. | 1987-01-07 | 203 | 0 |
| K863727 | FIXATION INSTRUMENTS | Medical Technology Development Corp. | 1986-10-31 | 38 | 0 |
| K863725 | CATARACT DIAMOND KNIFE | Medical Technology Development Corp. | 1986-10-31 | 38 | 0 |
| K863726 | INSTRUMENT STERILIZATION TRAY | Medical Technology Development Corp. | 1986-10-14 | 21 | 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