POST OAK INNOVATIONS, INC.

FDA Device Registration & Listing · Dallas, TX, US · Registration 3009770819

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009770819
FEI Number
3009770819
Entity Name
POST OAK INNOVATIONS, INC.
City/State/Country
Dallas, TX, US
Establishment Address
5327 N Central Expy Ste 300, Dallas, TX 75205, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Post Oak Innovations, Inc. (Owner Number: 10041495)
Owner / Operator Contact Address
5327 N. Central Expwy., St. 300, Dallas, TX 75205, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K112763
PMA Number
N/A

All Registered Proprietary Names

MatrixBrush tm Endometrial Sampler

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HFE Brush, Endometrial Obstetrics/Gynecology Class 2 884.1100 2012-07-30

Official Correspondent

Alexandra Gillespie

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Post Oak Innovations, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009770819. Last updated year: 2026. Please use registration number 3009770819 when referencing this establishment in official correspondence.
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