Data / Medical devices / Laparoscope, General & Plastic Surgery / France
FDA-registered makers of Laparoscope, General & Plastic Surgery in France: 6 establishments
6 establishments in France are registered with the FDA to make Laparoscope, General & Plastic Surgery (product code GCJ). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Laparoscope, General & Plastic Surgery
- Product code
- GCJ
- Country
- France
Makers of Laparoscope, General & Plastic Surgery in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sopro | LA CIOTAT CEDEX Bouches-du-Rhone, France | Manufacturer | 13 | April 1, 2009 | 0 | 0 | 0 | api.fda.gov |
| AB Medica SAS | Mery Sur Cher Centre-Val de Loire, France | Manufacturer, Repackager or relabeler | 3 | January 23, 2026 | 0 | 0 | 0 | api.fda.gov |
| Endocontrol | La Tronche Isere, France | Manufacturer | 1 | December 18, 2008 | 0 | 0 | 0 | api.fda.gov |
| Integra Microfrance SAS | SAINT AUBIN LE MONIAL Auvergne-Rhone-Alpes, France | Manufacturer | 1 | May 22, 2008 | 0 | 0 | 0 | api.fda.gov |
| Novatech S.A. | LA CIOTAT CEDEX Bouches-du-Rhone, France | Manufacturer | 1 | March 13, 2017 | 0 | 0 | 0 | api.fda.gov |
| Mauna Kea Technologies | PARIS Ile-de-France, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.