ENDOPLUS

FDA Device Registration & Listing · Mundelein, IL, US · Registration 1423714

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
1423714
FEI Number
3000719482
Entity Name
ENDOPLUS
City/State/Country
Mundelein, IL, US
Establishment Address
750 Tower Rd Ste A, Mundelein, IL 60060, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ENDOPLUS (Owner Number: 9005786)
Owner / Operator Contact Address
750 Tower Road, SUITE A, Mundelein, IL 60060, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K151567
PMA Number
N/A

All Registered Proprietary Names

Ruggles Reusable laparoscopic devices, inserts, handle and tube assemblies, coagulators, scissors, forceps Endoplus Hand-held Laparoscopic Instruments

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HBG Drills, Burrs, Trephines & Accessories (Manual) Neurology Class 2 882.4300 2013-01-30
HFI Coagulator, Culdoscopic (And Accessories) Obstetrics/Gynecology Class 2 884.4160 2007-11-21
HFI Coagulator, Culdoscopic (And Accessories) Obstetrics/Gynecology Class 2 884.4160 2015-12-29

Official Correspondent

Matthew Gudeman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ENDOPLUS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1423714. Last updated year: 2026. Please use registration number 1423714 when referencing this establishment in official correspondence.
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