Data / Medical devices / United States / Netbiologics LLC
Netbiologics LLC: FDA-registered device maker in Lakewood Ranch, FL, United States, 1 510(k) clearance
Netbiologics LLC is registered with the FDA (registration 3016778139) in Lakewood Ranch, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 23, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016778139
- Address
- 7912 Treesdale Glen, Lakewood Ranch, FL, United States, 34202
- Owner or operator
- netBiologics LLC (10092348)
- Roles
- Manufacturer
- First device listed
- December 28, 2024
- Registered through
- 2026
- Brand names listed
- Gaudi Proximal Humerus Plate, netBiologics
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Plate, Fixation, Bone | HRS | 2 | Manufacturer | accessdata.fda.gov |
| Screw, Fixation, Bone | HWC | 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 |
|---|---|---|---|---|---|---|
| July 23, 2024 | K241296 | Gaudi Proximal Humerus Plate | HRS | Substantially Equivalent | Netbiologics, LLC | accessdata.fda.gov |
Compare with other makers
Updated July 23, 2024. 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.