Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029300352

FEI Number

3029300352

Entity Name

Hubly Surgical

City/State/Country

Lisle, IL, US

Establishment Address

815 Ogden Ave, Lisle, IL 60532, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Hubly, Inc. (Owner Number: 10088698)

Owner / Operator Contact Address

815 Ogden Ave, Lisle, IL 60532, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K230619

PMA Number

N/A

All Registered Proprietary Names

Hubly Electric Drill

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HBE	Drills, Burrs, Trephines & Accessories (Simple, Powered)	Neurology	Class 2	882.4310	2023-10-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hubly, Inc.

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 3029300352. Last updated year: 2026. Please use registration number 3029300352 when referencing this establishment in official correspondence.