Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043527620

FEI Number

3043527620

Entity Name

RBC Development LLC dba RBC Medical Innovations dba Vantage MedTech

City/State/Country

Olathe, KS, US

Establishment Address

17100 W 118th Ter, Olathe, KS 66061, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Vantage Medtech (Owner Number: 10043154)

Owner / Operator Contact Address

17100 W 118th Terrace, Olathe, KS 66061, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Myriad SPECTRA Light Source - OUS Polaris Irrigation Pump Polaris Light Engine OsteoCool 2 RF Ablation System Accurian Claire OCT System B-Series OCT System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QFX	Diagnostic Neurosurgical Microscope Filter	Neurology	Class 2	882.4950	2024-07-15
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2024-04-08
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2024-04-02
GXI	Probe, Radiofrequency Lesion	Neurology	Class 2	882.4725	2019-03-05
GXD	Generator, Lesion, Radiofrequency	Neurology	Class 2	882.4400	2019-03-05
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2023-01-03
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2025-09-26
SHH	Oct Imaging System With Ai/Ml Software For Adjunctive Detection Of Breast Cancer	Unknown	Class 3	N/A	2026-06-01
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2026-06-18

Official Correspondent

Manju Kamath

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vantage Medtech

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3010126772	RBC Development LLC dba RBC Medical Innovations dba Vantage MedTech	Lenexa, KS, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17
K002257	Tecno Instruments (Pvt.) , Ltd.	TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100	2000-10-19
K193591	Bowa-Electronics GmbH & Co. KG	ARC 400	2020-04-02
K192128	Sutter Medizintechnik GmbH	Sutter Arrowtip Monopolar Electrodes	2019-10-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0720-2020	Abbott Medical	2	CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for the active tip. The active tip determines the size of the radiofrequency lesion.
Z-0664-2020	Abbott Medical	2	Radiofrequency Grounding Pad, REF RF-DGP-L

Similar Registrations

Registration Number	Establishment Name	Location
3010126772	RBC Development LLC dba RBC Medical Innovations dba Vantage MedTech	Lenexa, KS, US
3007456622	NICO CORPORATION	Indianapolis, IN, US
3015967359	Stryker Instruments	Portage, MI, US
9615010	CARL ZEISS MEDITEC AG (OBERKOCHEN)	OBERKOCHEN Baden-Wurttemberg, DE
3003974370	LEICA MICROSYSTEMS (SCHWEIZ) AG	HEERBRUGG Sankt Gallen, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043527620. Last updated year: 2026. Please use registration number 3043527620 when referencing this establishment in official correspondence.