Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031823122

FEI Number

3031823122

Entity Name

INQUIS MEDICAL, INC.

City/State/Country

Menlo Park, CA, US

Establishment Address

1530 O'Brien Drive, Suite A, Menlo Park, CA 94025, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Inquis Medical, Inc. (Owner Number: 10091176)

Owner / Operator Contact Address

1530 O'Brien Drive, Suite A, Menlo Park, CA 94025, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K240426

PMA Number

N/A

All Registered Proprietary Names

Aventus Thrombectomy System Aventus Thrombectomy System Aventus Introducer Sheath Aventus Thrombectomy System Aventus Clot Management System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KRA	Catheter, Continuous Flush	Cardiovascular	Class 2	870.1210	2024-07-17
QEW	Peripheral Mechanical Thrombectomy With Aspiration	Cardiovascular	Class 2	870.5150	2024-07-17
KRA	Catheter, Continuous Flush	Cardiovascular	Class 2	870.1210	2025-08-20
QEW	Peripheral Mechanical Thrombectomy With Aspiration	Cardiovascular	Class 2	870.5150	2025-08-20
DYB	Introducer, Catheter	Cardiovascular	Class 2	870.1340	2026-04-24
QEZ	Aspiration Thrombectomy Catheter	Cardiovascular	Class 2	870.5150	2026-03-09
CAC	Apparatus, Autotransfusion	Anesthesiology	Class 2	868.5830	2026-03-09
KRA	Catheter, Continuous Flush	Cardiovascular	Class 2	870.1210	2026-03-09
CAC	Apparatus, Autotransfusion	Anesthesiology	Class 2	868.5830	2024-07-17

Official Correspondent

Zachary Woodson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Inquis Medical, Inc.

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
K792141	Pharmaseal Div., Baxter Healthcare Corp.	CONTINUOUS FLUSH DEVICE	1979-12-05
K924661	Baxter Healthcare Corp	SWAN-GANZ INTELLICATH CCO THERMODILUTION CATHETER	1993-04-08
K241362	Surmodics,Inc.	Pounce XL Thrombectomy System (PTS-1011-7F135)	2024-09-11
K220887	Inari Medical	Mini-ClotTriever Thrombectomy System	2022-08-04
K250421	Inari Medical, Inc.	InThrill Thrombectomy System	2025-05-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0783-2020	Abbott Medical	2	Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303
Z-0789-2020	Abbott Medical	2	Fast-Cath Hemostasis Introducer, HEMOSTASIS INTRODUCER, 8.5F, 2.83 mm, REF 406143 - Product Usage: The Fast-Cath Hemostasis Introducers are indicated for the introduction of angiographic catheters, closed-end catheters, balloon catheters, and electrodes into a vessel where minimizing blood loss is essential.

Similar Registrations

Registration Number	Establishment Name	Location
3038791046	LIQUET MEDICAL INC.	Glen Allen, VA, US
3013134719	HEXACATH	Rueil Malmaison Ile-de-France, FR
3026567963	ENDOVASCULAR ENGINEERING, INC.	Menlo Park, CA, US
3021067373	VVT MED Ltd	Kfar Saba Central, IL
3019525998	VASCUPATENT MEDICAL (SHENZHEN) CO., LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031823122. Last updated year: 2026. Please use registration number 3031823122 when referencing this establishment in official correspondence.