MEDFINITI INTERNATIONAL,INC

FDA Device Registration & Listing · Las Vegas, NV, US · Registration 3021171301

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
3021171301
FEI Number
3021171301
Entity Name
MEDFINITI INTERNATIONAL,INC
City/State/Country
Las Vegas, NV, US
Establishment Address
10059 Prattville Ave, Las Vegas, NV 89148, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Medfiniti International, Inc (Owner Number: 10083258)
Owner / Operator Contact Address
400 N Ashley Dr, Ste 980, Tampa, FL 33602, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K023706
PMA Number
N/A

All Registered Proprietary Names

HemWell

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories) Gastroenterology, Urology Class 2 876.4300 2021-11-05

Official Correspondent

Michael Goeree

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Medfiniti International, 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
K172288 Wilson-Cook Medical Inc./Cook Endoscopy Fusion OMNI Sphincterotome 2018-04-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021171301. Last updated year: 2026. Please use registration number 3021171301 when referencing this establishment in official correspondence.
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