Medical Technology Development Corp.: FDA clearances and approvals
Medical Technology Development Corp. has 5 FDA 510(k) clearances (first 1986, latest 1994), across 5 product codes in 3 review panels. Median 510(k) review time: 38 days.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| EZL | Catheter, Retention Type, Balloon | 1 | 1 |
| FSM | Tray, Surgical, Instrument | 1 | 1 |
| HNN | Knife, Ophthalmic | 1 | 1 |
| HNR | Forceps, Ophthalmic | 1 | 1 |
| MOE | Collagen Corneal Shield | 1 | 1 |
Review panels
Most recent Medical Technology Development Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K941488 | DEVMED DOUBLE-BALLOON UROLOGICAL CATHETER | EZL | 1994-11-30 | 247 |
| K862315 | FYODOROV COLLAGEN CORNEAL SHIELD | MOE | 1987-01-07 | 203 |
| K863727 | FIXATION INSTRUMENTS | HNR | 1986-10-31 | 38 |
| K863725 | CATARACT DIAMOND KNIFE | HNN | 1986-10-31 | 38 |
| K863726 | INSTRUMENT STERILIZATION TRAY | FSM | 1986-10-14 | 21 |
Recalls
openFDA lists no recalls under a recalling firm named Medical Technology Development Corp..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Medical Technology Development Corp. have?
Medical Technology Development Corp. has 5 FDA 510(k) clearances (first 1986, latest 1994), across 5 product codes in 3 review panels.
How long does FDA take to clear Medical Technology Development Corp.'s 510(k)s?
The median time from FDA receipt to decision across Medical Technology Development Corp.'s cleared 510(k)s is 38 days.
What devices does Medical Technology Development Corp. make?
Its most frequent FDA product codes are EZL (Catheter, Retention Type, Balloon, 1); FSM (Tray, Surgical, Instrument, 1); HNN (Knife, Ophthalmic, 1).
Has Medical Technology Development Corp. had device recalls?
openFDA lists no recalls under a recalling firm name matching Medical Technology Development Corp. Related entities may recall under other names.
Next steps
- See all 5 Medical Technology Development Corp. clearances with predicates and recalls
- Run predicate analysis for product code EZL, Medical Technology Development Corp.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.