Data / Medical devices / United States / Post Oak Innovations, Inc.
Post Oak Innovations, Inc.: FDA-registered device maker in Dallas, TX, United States, 1 510(k) clearance
Post Oak Innovations, Inc. is registered with the FDA (registration 3009770819) in Dallas, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 18, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009770819
- Address
- 5327 N Central Expy Ste 300, Dallas, TX, United States, 75205
- Owner or operator
- Post Oak Innovations, Inc. (10041495)
- Roles
- Specification developer
- First device listed
- July 30, 2012
- Registered through
- 2026
- Brand names listed
- MatrixBrush tm Endometrial Sampler
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Endometrial | HFE | 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 |
|---|---|---|---|---|---|---|
| June 18, 2012 | K112763 | MATRIXBRUSH ENDOMETRIAL SAMPLER | HFE | Substantially Equivalent | Post Oak Innovations, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 18, 2012. 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.