CM Technologies, Inc.

FDA Device Registration & Listing · Carrollton, TX, US · Registration 3013524793

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
3013524793
FEI Number
3013524793
Entity Name
CM Technologies, Inc.
City/State/Country
Carrollton, TX, US
Establishment Address
1321 Valwood Parkway, Suite 530, Carrollton, TX 75006, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
CM Technologies, Inc. (Owner Number: 10049590)
Owner / Operator Contact Address
1321 Valwood Parkway,, Suite 530,, Carrollton, TX 75006, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Qora Stool Management Kit EnteralFit Qora Stool Managment Kit Qora Collection Bags QiVi Male External Urine Management Device QiVi Automated Urine Management Device QiVi Female External Urine Management Device AUM Drainage Tubing QiVi Acute Male External Urine Management Device AUM Canister Qoramatic, Qoramatic Drainage Bags QiVi Lite Male External Urine Management Device Qora Aeon Stool Management Kit Qora Collection Bags

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2022-03-11
NZU Collector, Urine, Powered, Non Indwelling Catheter Gastroenterology, Urology Class 1 876.5250 2020-05-04
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2021-10-06
NOA Device, Paste-On For Incontinence, Non-Sterile Gastroenterology, Urology Class 1 876.5250 2021-10-06
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2017-09-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CM Technologies, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011802696 QNQ Design and Development Pvt. Ltd. New Delhi, IN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K900590 Biosearch Medical Products, Inc. BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING 1990-08-02
K102548 Footprint Medical, Inc. FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE 2010-11-26
K955248 United States Endoscopy Group, Inc. U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT 1996-05-21
K872921 Medical Support, Inc. MSS ENTERAL DELIVERY SET 1987-12-03
K180622 Covidien Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port 2018-10-23

Similar Registrations

Registration Number Establishment Name Location
3025772870 ENTERAL ACCESS TECHNOLOGIES, LTD. Caerwys Flintshire, GB
3015237508 ADVANCED MEDICAL BALLOONS GMBH Waghaeusel Baden-Wurttemberg, DE
3009247326 Jabil Circuit (Singapore) Pte Ltd Singapore Central Singapore, SG
2528981 LYNX Medical Pennsylvania ERIE, PA, US
1649518 Sterigenics US LLC Fort Worth, TX, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013524793. Last updated year: 2026. Please use registration number 3013524793 when referencing this establishment in official correspondence.
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