Prexion Corporation
Chiyoda-Ku, JP
Prexion Corporation appears in FDA device records in Chiyoda-Ku, JP. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Prexion Corporation between 2016 and 2023. The busiest year on record is 2018, with 2. The most recent is 2023, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2016 | 1 |
| 2018 | 2 |
| 2019 | 1 |
| 2020 | 1 |
| 2021 | 1 |
| 2022 | 1 |
| 2023 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K232166 | PreXion3D Expedition | OAS | Substantially Equivalent | |
| K222150 | PreXion3D Expedition | OAS | Substantially Equivalent | |
| K221525 | PreXion3D Explorer PRO | OAS | Substantially Equivalent | |
| K203784 | PreXion3D Explorer PRO | OAS | Substantially Equivalent | |
| K193329 | PreXion3D Explorer EX | OAS | Substantially Equivalent | |
| K190320 | PreXion3D Explorer | OAS | Substantially Equivalent | |
| K181983 | PreXion 3D Excelsior | OAS | Substantially Equivalent | |
| K173878 | PreXion3D Excelsior | OAS | Substantially Equivalent | |
| K161881 | PreXion3D Excelsior | OAS | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain