Data / Medical devices / United States / Austin Medical Ventures, Inc.
Austin Medical Ventures, Inc.: FDA-registered device maker in Germantown, TN, United States, 1 510(k) clearance
Austin Medical Ventures, Inc. is registered with the FDA (registration 3013255153) in Germantown, TN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 30, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013255153
- Address
- 3012 Centre Oak Way Suite 102, Germantown, TN, United States, 38138
- Owner or operator
- Austin Medical Ventures, Inc. (10054360)
- Roles
- Specification developer
- First device listed
- March 10, 2017
- Registered through
- 2026
- Brand names listed
- Synthecure Calcium Sulfate
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Filler, Bone Void, Calcium Compound | MQV | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 30, 2003 | K031838 | PROFUSION BONE VOID FILLER KIT | MQV | Substantially Equivalent | Biogeneration | accessdata.fda.gov |
Compare with other makers
Updated October 30, 2003. 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.