Prexion Corporation: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Prexion Corporation” (first 2016, latest 2023), across 1 product code in 1 review panel. Median 510(k) review time under this name: 57 days. Since 2017 the median was 57 days, against 94 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2016 | 1 | 87 |
| 2017 | 0 | — |
| 2018 | 2 | 26 |
| 2019 | 1 | 61 |
| 2020 | 1 | 129 |
| 2021 | 1 | 57 |
| 2022 | 1 | 57 |
| 2023 | 2 | 112 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Prexion Corporation took a median 57 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 94 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| OAS | X-Ray, Tomography, Computed, Dental | 9 | 9 |
Review panels
- Radiology (9)
Most recent Prexion Corporation 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K232166 | PreXion3D Expedition | OAS | 2023-09-08 | 49 |
| K222150 | PreXion3D Expedition | OAS | 2023-01-12 | 176 |
| K221525 | PreXion3D Explorer PRO | OAS | 2022-07-22 | 57 |
| K203784 | PreXion3D Explorer PRO | OAS | 2021-02-23 | 57 |
| K193329 | PreXion3D Explorer EX | OAS | 2020-04-09 | 129 |
| K190320 | PreXion3D Explorer | OAS | 2019-04-15 | 61 |
| K181983 | PreXion 3D Excelsior | OAS | 2018-08-17 | 23 |
| K173878 | PreXion3D Excelsior | OAS | 2018-01-19 | 29 |
| K161881 | PreXion3D Excelsior | OAS | 2016-10-03 | 87 |
Recalls
openFDA lists no recalls under a recalling firm named Prexion Corporation.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Prexion Corporation?
FDA lists 9 510(k) clearances under the applicant name “Prexion Corporation” (first 2016, latest 2023), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Prexion Corporation?
The median time from FDA receipt to decision across 510(k)s cleared under the name Prexion Corporation is 57 days. Since 2017: 57 days, versus 94 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Prexion Corporation?
The most frequent FDA product codes under this applicant name are OAS (X-Ray, Tomography, Computed, Dental, 9).
Next steps
- See all 9 Prexion Corporation clearances with predicates and recalls
- Run predicate analysis for product code OAS, Prexion Corporation's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.