Data / Medical devices / United States / GSB LLC
GSB LLC: FDA-registered device maker in Nashville, TN, United States, 1 510(k) clearance
GSB LLC is registered with the FDA (registration 3013726944) in Nashville, TN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 6, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013726944
- Address
- 6301 Robin Hill RD, Nashville, TN, United States, 37205
- Owner or operator
- GSB LLC (10055269)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- June 28, 2017
- Registered through
- 2026
- Brand names listed
- Microtable
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Neurological Stereotaxic Instrument | HAW | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| March 6, 2014 | K132611 | MICROTABLE SYSTEM | HAW | Substantially Equivalent | Fred Haer Company, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 6, 2014. 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.