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FDA 510(k)

Diode Laser Hair Removal Machine (QDTM-03)

K-Number: K261692 · 2026-10-07

ApplicantBeijing Nubway S&T Co., Ltd.
Decision Date2026-10-07
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Diode Laser Hair Removal Machine (QDTM-03) is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Nubway S&T Co., Ltd.. It received FDA 510(k) clearance on 2026-10-07 under 510(k) number K261692. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Diode Laser Hair Removal Machine (QDTM-03)?

Diode Laser Hair Removal Machine (QDTM-03) is a medical device that received FDA 510(k) clearance on 2026-10-07. The listed applicant is Beijing Nubway S&T Co., Ltd.. The 510(k) number is K261692.

When did Diode Laser Hair Removal Machine (QDTM-03) receive FDA 510(k) clearance?

Diode Laser Hair Removal Machine (QDTM-03) received FDA 510(k) clearance on 2026-10-07, under 510(k) number K261692.

Who is the listed applicant for Diode Laser Hair Removal Machine (QDTM-03)?

The FDA 510(k) record lists Beijing Nubway S&T Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Diode Laser Hair Removal Machine (QDTM-03)?

The FDA product code for Diode Laser Hair Removal Machine (QDTM-03) is GEX. This falls under the Gastroenterology category.

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Other records listing Beijing Nubway S&T 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.

K261673LED Therapy Device (QLXY-01)K261841Q Switched Nd:YAG Laser machine (QLQW-01)K261693Diode laser hair removal machine (QDTM-04)K261674Skin Air Cooling System (QALF-01)K242951Diode laser hair removal machine (QDTM-02)K242943Q Switched Nd:YAG Laser machine (QNHF-01)

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Related Devices (Code: GEX)

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.

K262346CureLight Medical Diode Laser Systems (S3-BF45);CureLight Medical Diode Laser Systems (S2-B30);CureLight Medical Diode Laser Systems (S3-BF30);CureLight Medical Diode Laser Systems (S2-F15);CureLight Medical Diode Laser Systems (S2-H7.5)Wuhan Phomed Technology Co., Ltd.K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.

Official Source

View on FDA Database →

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

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