Cristcot LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3008627398

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
3008627398
FEI Number
3008627398
Entity Name
Cristcot LLC
City/State/Country
Austin, TX, US
Establishment Address
901 S. Mopac Expressway, Building 3, Suite 375, Austin, TX 78746, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cristcot LLC (Owner Number: 10033594)
Owner / Operator Contact Address
901 S. Mopac Expressway, Building 3, Suite 375, Austin, TX 78746, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sephure

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OOW Applicator For Rectal Suppository Gastroenterology, Urology Class 1 876.4730 2010-09-02

Official Correspondent

Jennifer Davagian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cristcot LLC
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 3008627398. Last updated year: 2026. Please use registration number 3008627398 when referencing this establishment in official correspondence.
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