actiTENS mini

Q: When was actiTENS mini cleared by the FDA?

actiTENS mini (K252767) received a 510(k) decision of Substantially Equivalent on January 16, 2026, 140 days after the submission was received.

Q: What is the product code of K252767?

The FDA product code is GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief, a Class II (moderate risk) device regulated under 21 CFR 882.5890.

FDA 510(k) K252767 · Sublimed

Substantially Equivalent

510(k) numberK252767

Submission

Device name: actiTENS mini
Applicant: Sublimed
Moirans, FR
Received: August 29, 2025
Decision date: January 16, 2026
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief
Device class: Class II (moderate risk)
Regulation: 21 CFR 882.5890
Specialty: Neurology

Other 510(k)s with product code GZJ

510(k)	Device	Applicant	Decision
K252712	STIMPOD NMS460 Nerve StimulatorGZJ · Traditional	Algiamed Technologies USA, Inc.	05/28/2026SE
K252236	CP Relief Wand Rx - TENS/NMESGZJ · Special	N & C Holdings, LLC	08/15/2025SE
K232441	Unipro (K-UNIPRO-US)GZJ · Traditional	Tenscare, Ltd.	08/30/2024SE
K241228	TENSWaveGZJ · Abbreviated	Zynex Medical Officer	08/27/2024SE
K233046	Electrical Neuromuscular Stimulator, Cure TrioGZJ · Traditional	Oriental Inspiration Limited	04/19/2024SE
K222879	Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)GZJ · Traditional	Wuxi Jiajian Medical Instrument Co., Ltd.	01/24/2023SE
K212618	iRelieve Microcurrent Pain Relief SystemGZJ · Traditional	Fast Track Technologies, Inc.	09/14/2022SE
K213802	StimOnTM Pain Relief System (GM2439)GZJ · Traditional	Gimer Medical Co., Ltd.	08/26/2022SE
K220578	Transcutaneous Electrical Nerve Stimulator (Model RJTENS-1)GZJ · Traditional	Bozhou Rongjian Medical Appliance Co., Ltd.	05/25/2022SE
K220503	TENS device-EmeTerm 2, Model: YF-ZTY-E2GZJ · Traditional	Wat Medical Technology, Inc.	04/23/2022SE

More from Wat Medical Technology, Inc.

510(k)	Device	Decision
K202159	actiTENSGZJ · Traditional	12/22/2020SE

Questions and answers

When was actiTENS mini cleared by the FDA?

actiTENS mini (K252767) received a 510(k) decision of Substantially Equivalent on January 16, 2026, 140 days after the submission was received.

What is the product code of K252767?

The FDA product code is GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief, a Class II (moderate risk) device regulated under 21 CFR 882.5890.