National Patent Development Corp.: FDA clearances and approvals
National Patent Development Corp. has 34 FDA 510(k) clearances (first 1977, latest 1985), across 20 product codes in 4 review panels. Median 510(k) review time: 33 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 |
|---|---|---|---|
| EIC | Syringe, Periodontic, Endodontic, Irrigating | 4 | 4 |
| FPA | Set, Administration, Intravascular | 4 | 4 |
| GAA | Needle, Aspiration And Injection, Disposable | 4 | 4 |
| EBF | Material, Tooth Shade, Resin | 2 | 2 |
| FMF | Syringe, Piston | 2 | 2 |
| KGX | Tape And Bandage, Adhesive | 2 | 2 |
| KIF | Resin, Root Canal Filling | 2 | 2 |
| KMF | Bandage, Liquid | 2 | 2 |
| BTO | Tube, Tracheostomy (W/Wo Connector) | 1 | 1 |
| BTR | Tube, Tracheal (W/Wo Connector) | 1 | 1 |
Plus 10 more product codes.
Review panels
- General and Plastic Surgery (12)
- Dental (9)
- General Hospital (9)
- Anesthesiology (3)
Most recent National Patent Development Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K843974 | VARIABLE TEMPERATURE CAUTERY DEVICE | GEI | 1985-02-26 | 138 |
| K832699 | HYDRON WOUND DRESSING FAST SEAT KIT | FRO | 1984-04-27 | 261 |
| K822793 | PIO ROOT CANAL INDICATOR | EIL | 1982-10-22 | 36 |
| K820028 | ZEON COMPOSITE RESIN LIGHT CURE SYS | EBF | 1982-03-11 | 65 |
| K820006 | ZEON COMPOSITE RESIN SYSTEM | EBF | 1982-01-22 | 18 |
| K811446 | HYDRON WOUND DRESSING KIT | KMF | 1981-06-12 | 21 |
| K801484 | ROOT CANAL FILLING APPLICATOR NEEDLES | EIC | 1980-07-21 | 66 |
| K801483 | MARK IV SYRINGE | EIC | 1980-07-21 | 66 |
| K801482 | HYDRON ROOT CANAL FILLING MATERIAL | KIF | 1980-07-21 | 66 |
| K792136 | HYPO-ALLERGENIC PLASTIC TAPE | FPX | 1980-01-16 | 86 |
24 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named National Patent 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 National Patent Development Corp. have?
National Patent Development Corp. has 34 FDA 510(k) clearances (first 1977, latest 1985), across 20 product codes in 4 review panels.
How long does FDA take to clear National Patent Development Corp.'s 510(k)s?
The median time from FDA receipt to decision across National Patent Development Corp.'s cleared 510(k)s is 33 days.
What devices does National Patent Development Corp. make?
Its most frequent FDA product codes are EIC (Syringe, Periodontic, Endodontic, Irrigating, 4); FPA (Set, Administration, Intravascular, 4); GAA (Needle, Aspiration And Injection, Disposable, 4).
Has National Patent Development Corp. had device recalls?
openFDA lists no recalls under a recalling firm name matching National Patent Development Corp. Related entities may recall under other names.
Next steps
- See all 34 National Patent Development Corp. clearances with predicates and recalls
- Run predicate analysis for product code EIC, National Patent 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.