Data / Medical devices / France / Dilon Technologies France SAS
Dilon Technologies France SAS: FDA-registered device maker in St Priest Rhone, France, 1 PMA approval
Dilon Technologies France SAS is registered with the FDA (registration 3007702492) in St Priest Rhone, France. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated December 15, 2017. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007702492
- Address
- 8 Allee Irene Joliot Curie, St Priest Rhone, France, 69800
- Owner or operator
- DILON TECHNOLOGIES Inc (9035906)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- October 17, 2022
- Registered through
- 2026
- Brand names listed
- HEMOBLAST Bellows
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorbable Collagen Hemostatic Agent With Thrombin | PMX | 3 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| December 15, 2017 | P170012 | HEMOBLAST Bellows | PMX | 32 | September 3, 2026 | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| December 2, 2016 | 76319 | Class II | Terminated | RENOVIX Guided Healing Collagen Membrane Intended for use in oral surgical procedures. | Lack of sterility assurance | accessdata.fda.gov |
Compare with other makers
Updated September 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.