InterX Technologies

Plano, TX, US

InterX Technologies appears in FDA device records in Plano, TX. FDA records list 4 510(k) clearances between 2005-05-17 and 2013-06-21, no PMA records and one registered establishment. As of 2026-09-10, FDA records show one recall for this company, and at least one establishment registration is current.

510(k) clearances: 4
PMA records: 0
Recall records: 1
Registered establishments: 1

FDA records under these names

1 name

FDA records resolved to InterX Technologies carry these names as well, as FDA wrote them. Each is the firm named on a registration, a 510(k), a PMA, a recall or an enforcement report that was joined to this company on a shared FDA identifier or on a matching name.

Neuro Resource Group, Inc.510(k), recall

510(k) clearance history

FDA records hold 4 510(k) clearances for InterX Technologies between 2005 and 2013. The busiest year on record is 2005, with 1. The most recent is 2013, with 1.

Clearances by year, as a table

510(k) clearance decisions for InterX Technologies, by decision year
Year	Clearances
2005	1
2006	1
2008	1
2013	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K130816	INTERX STERILE SELF-ADHESIVE DUAL ELECTRODE (ISSDE)	GXY	Substantially Equivalent	2013-06-21
K070217	INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE	NFO	Substantially Equivalent	2008-04-04
K053626	INTERX500 FLEXIBLE ARRAY ELECTRODE	GXY	Substantially Equivalent	2006-03-29
K042912	INTERX5000	GZJ	Substantially Equivalent	2005-05-17

Registered establishments

FDA registered establishments for InterX Technologies, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3004786509	3004786509	InterX Technologies	3465 Technology Dr., Suite A, Plano, TX 75074 US	2026	GXY GZJ NFO

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
Recall	Product	Reason	Classification	Initiated	Status
Z-2105-2011	Inter x 5002 Device, Inter x Professional Sport Device, Inter x 1000 Personal Device, and Inter x Personal Sport packaged with Triad alcohol wipes. The alcohol wipes manufactured by the Triad Group were labeled under brand names Triad, Select, Select Medical Products, PSS Select or PSS World Medical Inc. Alcohol wipe is provided as a cleaning convenience for device electrodes.	Product package contains alcohol prep pads recalled by Triad Group because the prep pads have the potential to be contaminated with an objectionable organism.		2011-02-07	Terminated

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain