Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2024292

FEI Number

2024292

Entity Name

BioMedical Life Systems Inc.

City/State/Country

Carlsbad, CA, US

Establishment Address

1954 Kellogg Avenue, Carlsbad, CA 92008, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

BioMedical Life Systems Inc. (Owner Number: 10027823)

Owner / Operator Contact Address

1954 Kellogg Ave, Carlsbad, CA 92008, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K061476

PMA Number

N/A

All Registered Proprietary Names

EMS 2000 QuadStar II Rebound Sport Rebound Rebound Health Pain Buddy Micro Plus GV350 Impulse 3000 T Impulse 3000T BioMed 2000 XT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2008-12-04
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2008-12-04
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2008-12-04
LIH	Interferential Current Therapy	Neurology	Class 2	882.5890	2008-12-04
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2011-10-13
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2008-12-04
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2008-12-04
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2008-12-04
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2008-12-04

Official Correspondent

Derick Corrente

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BioMedical Life Systems 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
K030403	Cefar Medical AB	CEFAR REHAB 2 AND REHAB 2 PRO	2003-07-17
K231440	Shenzhen Roundwhale Technology Co. , Ltd.	Combo Electrotherapy Device	2023-11-03
K820884	Nitron Electronics	ELECTRICAL MUSCLE STIMULATOR	1982-04-29
K201958	Therasigma, LLC	ETD Family of Electrotherapy Devices	2020-08-04
K964028	Mettler Electronics Corp.	SYS STIM 226	1997-02-03

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3038295706	JUST KEEP HEALTHY CO., LTD.	Samkkei Munichay District Kampong Speu, KH
3019892999	CIONIC Facility	Scotts Valley, CA, US
3012316249	COMPASS HEALTH BRANDS (CORPORATE OFFICE)	Middleburg Heights, OH, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2024292. Last updated year: 2026. Please use registration number 2024292 when referencing this establishment in official correspondence.