Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023805

FEI Number

3023805

Entity Name

LEANDER, LLC

City/State/Country

Lawrence, KS, US

Establishment Address

1400 E 24th St Ste C, Lawrence, KS 66046, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Leander, LLC (Owner Number: 3023805)

Owner / Operator Contact Address

1400 E. 24th Street, SUITE C, Lawrence, KS 66046, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Flexion Distraction Table

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LGX	Table, Examination, Medical, Powered	General, Plastic Surgery	Class 1	878.4960	1992-12-17

Official Correspondent

Gary Summers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Leander, LLC

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

View Entity Profile →

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3015978022	INSPITAL MEDICAL TECHNOLOGY GMBH	Neuss North Rhine-Westphalia, DE
3017181414	JIANGSU YONGFA MEDICAL EQUIPMENT TECHNOLOGY CO., LTD	Zhangjiagang City Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023805. Last updated year: 2026. Please use registration number 3023805 when referencing this establishment in official correspondence.