Data / Medical devices / United States / Technical Services For Electronics, Inc.

Technical Services For Electronics, Inc.: FDA-registered device maker in Jackson, MN, United States, 1 PMA approval

Name: Technical Services For Electronics, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Technical Services For Electronics, Inc. is registered with the FDA (registration 2135338) in Jackson, MN, United States. It lists 27 device types. The FDA files 1 PMA approval under its listings, the newest dated February 9, 1995. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 2135338
FEI number: 3005700659
Address: 177 Industrial Parkway, Jackson, MN, United States, 56143
Owner or operator: TECHNICAL SERVICES FOR ELECTRONICS, INC. (9044482)
Roles: Contract manufacturer, Repackager or relabeler
First device listed: January 5, 2011
Registered through: 2026
Brand names listed: ECG Trunk Cables and Leadwires, EnSite X EP System Connect Cable, EnSite X EP System Radio-lucent ECG Lead set, EnSite X EP System Radio-opaque ECG Lead set, EnSite X EP System SurfaceLink Module, MDT-Neuro (Stimulator Programmer/Recharger) Antenna, Merlin TM PSA Patient Cable - EX3150, Model 4806L15 Foot Switch and more

Devices it lists

Device	Product code	Class	Role	Source
Cable, Electrode	IKD	2	Contract manufacturer	accessdata.fda.gov
Cable, Transducer And Electrode, Patient, (Including Connector)	DSA	2	Contract manufacturer	accessdata.fda.gov
Cardiac Ablation Percutaneous Catheter	LPB	3	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Catheter, Electrode Recording, Or Probe, Electrode Recording	DRF	2	Contract manufacturer	accessdata.fda.gov
Computer, Diagnostic, Programmable	DQK	2	Contract manufacturer	accessdata.fda.gov
Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)	OLM	f	Contract manufacturer	accessdata.fda.gov
Electrode, Pacemaker, Temporary	LDF	2	Contract manufacturer	accessdata.fda.gov
Implantable Cardioverter Defibrillator (Non-Crt)	LWS	3	Contract manufacturer	accessdata.fda.gov
Implantable Pacemaker Pulse-Generator	DXY	3	Contract manufacturer	accessdata.fda.gov
Implantable Pulse Generator, Pacemaker (Non-Crt)	LWP	3	Contract manufacturer	accessdata.fda.gov
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence	QON	3	Contract manufacturer	accessdata.fda.gov
Implanted Subcortical Electrical Stimulator (Motor Disorders)	MRU	f	Contract manufacturer	accessdata.fda.gov
Neuromodulator For Obesity	PIM	3	Contract manufacturer	accessdata.fda.gov
Pacemaker/Icd/Crt Non-Implanted Components	OSR	3	Contract manufacturer	accessdata.fda.gov
Programmer, Pacemaker	KRG	3	Contract manufacturer	accessdata.fda.gov
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)	NKE	3	Contract manufacturer	accessdata.fda.gov
Pulse Generator, Permanent, Implantable	NVZ	3	Contract manufacturer	accessdata.fda.gov
Pump, Infusion, Implanted, Programmable	LKK	3	Contract manufacturer	accessdata.fda.gov
Stimulator, Electrical, Implantable, For Incontinence	EZW	3	Contract manufacturer	accessdata.fda.gov
Stimulator, Electrical, Implanted, For Parkinsonian Symptoms	NHL	3	Contract manufacturer	accessdata.fda.gov
Stimulator, Electrical, Implanted, For Parkinsonian Tremor	MHY	3	Contract manufacturer	accessdata.fda.gov
Stimulator, Peripheral Nerve, Implanted (Pain Relief)	GZF	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Spinal-Cord, Implanted (Pain Relief)	GZB	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief	LGW	3	Contract manufacturer	accessdata.fda.gov
Stimulator, Thalamic, Epilepsy, Implanted	MBX	3	Contract manufacturer	accessdata.fda.gov
Tester, Pacemaker Electrode Function	DTA	2	Contract manufacturer	accessdata.fda.gov
Wearable Automated External Defibrillator	MVK	3	Contract manufacturer	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
February 9, 1995	P930029	ATAKR(TM) RFCA SYSTEM	LPB	66	July 1, 2024	accessdata.fda.gov

Compare with other makers

Updated July 1, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.