STIMPOD NMS460 Nerve Stimulator
FDA 510(k) K252712 · Algiamed Technologies USA, Inc.
510(k) numberK252712
Submission
- Device name
- STIMPOD NMS460 Nerve Stimulator
- Applicant
- Algiamed Technologies USA, Inc.
Lake Mary, FL, US - Received
- August 27, 2025
- Decision date
- May 28, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code GZJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252767 | actiTENS miniGZJ · Traditional | Sublimed | 01/16/2026SE |
| 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 |
Questions and answers
When was STIMPOD NMS460 Nerve Stimulator cleared by the FDA?
STIMPOD NMS460 Nerve Stimulator (K252712) received a 510(k) decision of Substantially Equivalent on May 28, 2026, 274 days after the submission was received.
What is the product code of K252712?
The FDA product code is GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief, a Class II (moderate risk) device regulated under 21 CFR 882.5890.