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FDA 510(k)

TENS 7000 Rechargeable 4 Channel (TENS 7000H)

K-Number: K260412 · 2026-06-26

Decision Date2026-06-26
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS 7000 Rechargeable 4 Channel (TENS 7000H) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongdixin Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-06-26 under 510(k) number K260412. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENS 7000 Rechargeable 4 Channel (TENS 7000H)?

TENS 7000 Rechargeable 4 Channel (TENS 7000H) is a medical device that received FDA 510(k) clearance on 2026-06-26. The listed applicant is Shenzhen Dongdixin Technology Co., Ltd.. The 510(k) number is K260412.

When did TENS 7000 Rechargeable 4 Channel (TENS 7000H) receive FDA 510(k) clearance?

TENS 7000 Rechargeable 4 Channel (TENS 7000H) received FDA 510(k) clearance on 2026-06-26, under 510(k) number K260412.

Who is the listed applicant for TENS 7000 Rechargeable 4 Channel (TENS 7000H)?

The FDA 510(k) record lists Shenzhen Dongdixin Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS 7000 Rechargeable 4 Channel (TENS 7000H)?

The FDA product code for TENS 7000 Rechargeable 4 Channel (TENS 7000H) is NUH.

Other records listing Shenzhen Dongdixin Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 10 devices →

Related Devices (Code: NUH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.