IDEATE MEDICAL

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3043237009

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
3043237009
FEI Number
3043237009
Entity Name
IDEATE MEDICAL
City/State/Country
Saint Louis, MO, US
Establishment Address
2821 N Ballas Rd Ste C55, Saint Louis, MO 63131, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
IDEATE MEDICAL (Owner Number: 10095230)
Owner / Operator Contact Address
2821 N. Ballas Road C55, Saint Louis, MO 63131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Suction Connector Assembly Type 2 Insert Connector Assembly Small Type 1 Pipette Connector Type 3 Suction Connector Assembly Type 3 SteroScope Container Sterilization Filter SteroScope Basket SteroScope Sterilization Technology SteroScope Container SteroScope Sterilant Water Supply Connector Type 2 Insert Connector Assembly Large Type 2 Pipette Connector Type 1 Luer Connector Type 1 Biopsy Connector Type 1 Insert Connector Medium Type 1 Pipette Connector Type 2 Biopsy Connector Type 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MLR Sterilizer, Chemical General Hospital Class 2 880.6860 2026-02-09
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories General Hospital Class 2 880.6850 2026-02-09

Official Correspondent

William Wong

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

IDEATE MEDICAL
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
K243425 Talladium España, SL Guided DAS Surgical Kit 2025-07-22
K213209 K1 Medical, LLC EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device 2021-12-28
K012105 Symmetry Medical, Inc. POLYVAC SURGICAL INSTRUMENT DELIVERY SYSTEM 2002-08-02
K243317 Infinitum Eta, Ltd. NUVENTUS NV.C™ Surgical Cassette and Tray 2025-02-11
K112536 Covidien SONICISION STERILIZATION TRAY 2012-04-19

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0043-2014 Advanced Sterilization Products 2
STERRAD 200 Sterilizer (Single Door), Part Number: 10201. STERRAD 200 Sterilizer (Double Door), Part Number: 10202. The STERRAD Sterilization System is a low temperature general purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.
Z-0044-2014 Advanced Sterilization Products 2
STERRAD 100NX Cassettes The STERRAD Sterilization System is a low temperature general purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.

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3015207155 Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai, CN
3003950207 STERIS Corporation Mentor, OH, US
3016075971 Plasmapp Co., Ltd. Asan-si Chungnam, KR
3005899764 STERIS MEXICO, S. de R.L. de C.V. GUADALUPE Nuevo Leon, MX
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043237009. Last updated year: 2026. Please use registration number 3043237009 when referencing this establishment in official correspondence.
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