Axess Vision Technology
Joue Les Tours Indre-et-Loire, FR
AXESS VISION TECHNOLOGY appears in FDA device records in Joue Les Tours Indre-et-Loire, FR. FDA records list 2 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 2 510(k) clearances for Axess Vision Technology between 2020 and 2022. The busiest year on record is 2020, with 1. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2020 | 1 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K212886 | Broncoflex Agile, Broncoflex Vortex, Screeni | EOQ | Substantially Equivalent | |
| K202180 | Broncoflex Agile; Product Reference: 20030001 , Broncoflex Vortex; Product Reference: 10030001, Screeni; Product Reference: 30030001 | EOQ | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3017859830 | 3017859830 | AXESS VISION TECHNOLOGY | Zone de la Liodiere, Joue Les Tours Indre-et-Loire 37300 FR | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
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