Dyna Corp.: FDA clearances and approvals
Dyna Corp. has 5 FDA 510(k) clearances (first 1990, latest 1997), across 2 product codes in 1 review panel. Median 510(k) review time: 56 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 |
|---|---|---|---|
| FPO | Stretcher, Wheeled | 3 | 3 |
| FPP | Stretcher, Hand-Carried | 2 | 2 |
Review panels
- General Hospital (5)
Most recent Dyna Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K972528 | DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759) | FPO | 1997-07-28 | 21 |
| K962181 | HARE MODEL 2000 EZ LOADER MODEL 95555 | FPO | 1996-08-01 | 56 |
| K902503 | HARE FOLDING BACK EMERGENCY STRETCHER | FPO | 1990-06-26 | 21 |
| K900671 | HARE EMERGENCY STRETCHER WITH WHEELS | FPP | 1990-04-23 | 69 |
| K900670 | HARE EMERGENCY STRETCHER | FPP | 1990-04-23 | 69 |
Recalls
openFDA lists no recalls under a recalling firm named Dyna 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 Dyna Corp. have?
Dyna Corp. has 5 FDA 510(k) clearances (first 1990, latest 1997), across 2 product codes in 1 review panel.
How long does FDA take to clear Dyna Corp.'s 510(k)s?
The median time from FDA receipt to decision across Dyna Corp.'s cleared 510(k)s is 56 days.
What devices does Dyna Corp. make?
Its most frequent FDA product codes are FPO (Stretcher, Wheeled, 3); FPP (Stretcher, Hand-Carried, 2).
Has Dyna Corp. had device recalls?
openFDA lists no recalls under a recalling firm name matching Dyna Corp. Related entities may recall under other names.
Next steps
- See all 5 Dyna Corp. clearances with predicates and recalls
- Run predicate analysis for product code FPO, Dyna 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.