Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1722684

FEI Number

1000220650

Entity Name

CLINICAL INNOVATIONS, LLC

City/State/Country

MURRAY, UT, US

Establishment Address

747 W 4170 S, MURRAY, UT 84123, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Clinical Innovations, LLC (Owner Number: 10035300)

Owner / Operator Contact Address

747 W 4170 S, Murray, UT 84123, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Kiwi Complete Vacuum Delivery System LifeBubble Koala Intrauterine Pressure Catheter Koala BoogieBaby Kiwi Traxi Panniculus Retractor Clearview Uterine Manipulator AccuCirc babyLance Eclipse System AIR-CHARGED CATHETERS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HDB	Extractor, Vacuum, Fetal	Obstetrics/Gynecology	Class 2	884.4340	2025-12-09
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2025-05-14
HFN	Transducer, Pressure, Intrauterine	Obstetrics/Gynecology	Class 2	884.2700	2025-06-09
HFN	Transducer, Pressure, Intrauterine	Obstetrics/Gynecology	Class 2	884.2700	2011-02-17
BYY	Tube, Aspirating, Flexible, Connecting	General Hospital	Class 2	880.6740	2020-12-04
HDB	Extractor, Vacuum, Fetal	Obstetrics/Gynecology	Class 2	884.4340	2011-02-17
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2015-01-14
LKF	Cannula, Manipulator/Injector, Uterine	Obstetrics/Gynecology	Class 2	884.4530	2011-02-17
HFX	Clamp, Circumcision	Obstetrics/Gynecology	Class 2	884.4530	2011-02-17
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2023-03-08
PJH	Dynamic Rectal Control System	Gastroenterology, Urology	Class 2	876.5930	2022-05-24
FEN	Device, Cystometric, Hydraulic	Gastroenterology, Urology	Class 2	876.1620	2011-02-17

Official Correspondent

Nicole Boser

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Clinical Innovations, 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
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-05	CooperSurgical, Inc.	2	Mystic M-Style Mushroom Cup Mityvac Vacuum Assisted Delivery System Product No: 10047
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1722684. Last updated year: 2026. Please use registration number 1722684 when referencing this establishment in official correspondence.