Data / Medical devices / France / Aesthetic Group
Aesthetic Group: FDA-registered device maker in Puiseux Le Hauberger Oise, France, 3 510(k) clearances
Aesthetic Group is registered with the FDA (registration 3007279404) in Puiseux Le Hauberger Oise, France. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 27, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007279404
- Address
- Rue De Bornel Za La Gobette, Puiseux Le Hauberger Oise, France, 60540
- Owner or operator
- Aesthetic Group (10042355)
- Roles
- Exporter to the US, Foreign private label distributor, Manufacturer
- First device listed
- November 18, 2012
- Registered through
- 2026
- Brand names listed
- 1 ml LDS syringe, FINE-JECT, Infiltration kit, Injection cannula, Kipic, LIPO-one, Lipofilling kit, VacLok
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Plastic Surgery And Accessories Kit | FTN | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Foreign private label distributor | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Foreign private label distributor | accessdata.fda.gov |
| System, Suction, Lipoplasty For Removal | QPB | 2 | Manufacturer | accessdata.fda.gov |
| Vacuum Syringe | PUR | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 27, 2017 | K163597 | VacLok AT Vacuum Syringe | PUR | Substantially Equivalent | Merit Medical Systems, Inc. | accessdata.fda.gov |
| July 30, 2014 | K132353 | SUCTION LIPOPLASTY ACCESSORIES | QPB | Substantially Equivalent | Inex | accessdata.fda.gov |
| October 30, 1998 | K983067 | FINE-JECT | FMI | Substantially Equivalent | Henke Sass Wolf of America, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Plastic Surgery And Accessories Kit
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Piston
- All makers of System, Suction, Lipoplasty For Removal
- All makers of Cannula, Surgical, General & Plastic Surgery
Updated July 27, 2017. 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.