Century HLM, LLC

FDA Device Registration & Listing · Saint Charles, MO, US · Registration 3001589655

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
3001589655
FEI Number
3001589655
Entity Name
Century HLM, LLC
City/State/Country
Saint Charles, MO, US
Establishment Address
3551 Somerset Hills Dr, Saint Charles, MO 63303, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Century HLM, LLC (Owner Number: 9066037)
Owner / Operator Contact Address
3551 Somerset Hills Drive, --, Saint Charles, MO 63303, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202125
PMA Number
N/A

All Registered Proprietary Names

Century Century Perfusion System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWB Pump, Blood, Cardiopulmonary Bypass, Roller Type Cardiovascular Class 2 870.4370 2007-12-07
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass Cardiovascular Class 2 870.4220 2021-07-27

Official Correspondent

JEFF POLAND

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Century HLM, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K822071 Gambro, Inc. PUMP MODULES PMO LO-110-PMD 10-210 1982-08-24

Similar Registrations

Registration Number Establishment Name Location
3042990265 MEDIYANT TECHNOLOGIES PRIVATE LIMITED Vadodara Gujarat, IN
1828100 TERUMO CARDIOVASCULAR SYSTEMS CORPORATION ANN ARBOR, MI, US
2916596 THORATEC CORP. PLEASANTON, CA, US
3019807891 CENTERPIECE S. DE R.L DE C.V (sterilization site) Tijuana Baja California, MX
9611109 LivaNova Deutschland GmbH MUNCHEN Bavaria, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001589655. Last updated year: 2026. Please use registration number 3001589655 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.