ASR SYSTEMS, INC.

FDA Device Registration & Listing · San Antonio, TX, US · Registration 3019315238

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
3019315238
FEI Number
3019315238
Entity Name
ASR SYSTEMS, INC.
City/State/Country
San Antonio, TX, US
Establishment Address
14439 NW Military Hwy., Ste. 108 - 469, San Antonio, TX 78231, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
ASR Systems, Inc. (Owner Number: 10081985)
Owner / Operator Contact Address
14439 NW Military Hwy., Ste. 108 - 469, San Antonio, TX 78231, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TITAN CSR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FFO Retractor, Self-Retaining Gastroenterology, Urology Class 1 876.4730 2021-06-02

Official Correspondent

Mike Girouard

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ASR Systems, 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 3019315238. Last updated year: 2026. Please use registration number 3019315238 when referencing this establishment in official correspondence.
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