INVENTEUR, LLC

FDA Device Registration & Listing · Saint Petersburg, FL, US · Registration 3038913749

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
3038913749
FEI Number
3038913749
Entity Name
INVENTEUR, LLC
City/State/Country
Saint Petersburg, FL, US
Establishment Address
7901 4th St N Ste 300, Saint Petersburg, FL 33702, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Inventeur, LLC (Owner Number: 10093634)
Owner / Operator Contact Address
7901 4th St N, STE 300, Saint Petersburg, FL 33702, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K240937
PMA Number
N/A

All Registered Proprietary Names

Anesthesia Intraoral Module (AIM)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAT Cannula, Nasal, Oxygen Anesthesiology Class 1 868.5340 2025-06-15
MNK Endoscopic Bite Block Gastroenterology, Urology Class 1 876.1500 2025-06-15
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase Anesthesiology Class 2 868.1400 2025-06-15

Official Correspondent

TARIQ CHAUDHRY

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Inventeur, 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
K142467 Abeon Medical Corporation IntelAir Nasal Airway Support System 2014-11-24
K861213 Datex Division Instrumentarium Corp. PB 254 IR - SPECTROMETER 1986-04-04
K172904 Philips Medizin Systeme Boeblingen GmbH IntelliVue Capnography Extension, IntelliVue Microstream Extension 2017-12-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0021-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N, Part Number CS08651-01
Z-0024-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657
Z-0025-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02
Z-0026-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01
Z-0027-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038913749. Last updated year: 2026. Please use registration number 3038913749 when referencing this establishment in official correspondence.
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