Data / Medical devices / France / NG Biotech
NG Biotech: FDA-registered device maker in GUIPRY Bretagne, France, 2 510(k) clearances
NG Biotech is registered with the FDA (registration 3012516784) in GUIPRY Bretagne, France. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 4, 2025. Registered through 2026. 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.
- FDA registration number
- 3012516784
- Address
- ZA Courbouton Secteur 1, GUIPRY Bretagne, France, 35480
- Owner or operator
- NG BIOTECH (10061777)
- Roles
- Manufacturer
- First device listed
- November 20, 2019
- Registered through
- 2026
- Brand names listed
- NG-Test CARBA 5, NG-Test CTX-M Multi
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Phenotypic Test Kit, Non-Susceptible/Elevated Mic Organisms, Cultured Isolates | PTJ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| June 4, 2025 | K243499 | NG-Test® CTX-M MULTI | PTJ | Substantially Equivalent | Ng Biotech | accessdata.fda.gov |
| October 2, 2019 | K191889 | NG-Test CARBA 5 | PTJ | Substantially Equivalent | Ng Biotech | accessdata.fda.gov |
Updated June 4, 2025. 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.