MOTUS GI Inc

FDA Device Registration & Listing · Fort Lauderdale, FL, US · Registration 3013184907

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
3013184907
FEI Number
3013184907
Entity Name
MOTUS GI Inc
City/State/Country
Fort Lauderdale, FL, US
Establishment Address
1301 E Broward Blvd, Suite 310, Fort Lauderdale, FL 33301, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
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
Y
Expiration Date (Year)
2026
510(k) Number
K220007
PMA Number
N/A

All Registered Proprietary Names

Endoscopy Cart Pure-Vu EVS System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOX Stand, Infusion General Hospital Class 1 880.6990 2019-06-28
FDF Colonoscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2022-02-23

Official Correspondent

Mark Pomeranz

US Agent Details

No US Agent registered (Local establishment).

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
3011816755 MOTUS GI Medical Technologies Ltd. Tirat Carmel Haifa, IL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013184907. Last updated year: 2026. Please use registration number 3013184907 when referencing this establishment in official correspondence.
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