Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011816755

FEI Number

3011816755

Entity Name

MOTUS GI Medical Technologies Ltd.

City/State/Country

Tirat Carmel Haifa, IL

Establishment Address

22 Keren Ha'yesod st., Tirat Carmel Haifa 3902638, IL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

MOTUS GI Medical Technologies Ltd (Owner Number: 10053317)

Owner / Operator Contact Address

1301 E. Broward Blvd., Suite 310, Fort Lauderdale, FL 33301, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pure-Vu EVS System Pure-Vu EVS Waste Bag Endoscopy Cart

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FDS	Gastroscope And Accessories, Flexible/Rigid	Gastroenterology, Urology	Class 2	876.1500	2024-12-03
FDF	Colonoscope And Accessories, Flexible/Rigid	Gastroenterology, Urology	Class 2	876.1500	2024-12-03
KDQ	Bottle, Collection, Vacuum	General Hospital	Class 2	880.6740	2026-04-21
FOX	Stand, Infusion	General Hospital	Class 1	880.6990	2019-06-28

Official Correspondent

Mark Pomeranz

US Agent Details

Mark Pomeranz Business: Motus GI Email: mark@motusgi.com Phone: (941) 5418000

Related Public Records

Same Entity

MOTUS GI Medical Technologies Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3013184907	MOTUS GI Inc	Fort Lauderdale, FL, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K232314	FUJIFILM Healthcare Americas Corporation	Hood (DH-106STL, DH-116STL, DH-126STL, DH-096ST)	2023-09-01

Similar Registrations

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3004837686	Micro-Tech (Nanjing) Co., Ltd.	NAN JING Jiangsu, CN
2020550	KARL STORZ ENDOSCOPY-AMERICA, INC.	Auburn, MA, US
3015136743	STERI-TECH CO.,LTD.	KAZO-SHI Saitama, JP
3008797804	ALTON SHANGHAI MEDICAL INSTRUMENTS CO LTD	Shanghai, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011816755. Last updated year: 2026. Please use registration number 3011816755 when referencing this establishment in official correspondence.