Data / Medical devices / Germany / Ngmedical GMBH
Ngmedical GMBH: FDA-registered device maker in Nonnweiler Saarland, Germany, 7 510(k) clearances
Ngmedical GMBH is registered with the FDA (registration 3017065977) in Nonnweiler Saarland, Germany. It lists 2 device types. The FDA files 7 510(k) clearances under its listings, the newest dated April 30, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017065977
- Address
- Trierer Strasse 65, Nonnweiler Saarland, Germany, 66620
- Owner or operator
- NGMedical GmbH (10079411)
- Roles
- Manufacturer, Specification developer
- First device listed
- February 10, 2021
- Registered through
- 2026
- Brand names listed
- BEE Cages, BEE HA Extension, BEE PLIF, BEE PLIF Extension, BEE-HA, BEE-short, NGM WAVE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Intervertebral Fusion Device With Bone Graft, Cervical | ODP | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Lumbar | MAX | 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 |
|---|---|---|---|---|---|---|
| April 30, 2026 | K261067 | BEE PLIF Cage | MAX | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| November 21, 2025 | K250560 | BEE HA | ODP | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| January 12, 2024 | K231371 | BEE Cervical Cage | ODP | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| December 1, 2021 | K212050 | NGM WAVE PLIF Cage | MAX | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| August 27, 2021 | K211413 | BEE PLIF Cage | MAX | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| March 18, 2021 | K203444 | BEE HA Cage | ODP | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
| January 29, 2021 | K200429 | BEE Cages | ODP | Substantially Equivalent | NGMedical GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Intervertebral Fusion Device With Bone Graft, Cervical
- All makers of Intervertebral Fusion Device With Bone Graft, Lumbar
Updated April 30, 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.