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FDA 510(k)

Sensilift Pro (ST300XXYYZZZ)

K-Number: K250341 · 2026-01-06

ApplicantEl Global Trade, Ltd.
Decision Date2026-01-06
Product CodePAY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Sensilift Pro (ST300XXYYZZZ) is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2026-01-06 under 510(k) number K250341. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sensilift Pro (ST300XXYYZZZ)?

Sensilift Pro (ST300XXYYZZZ) is a medical device that received FDA 510(k) clearance on 2026-01-06. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K250341.

When did Sensilift Pro (ST300XXYYZZZ) receive FDA 510(k) clearance?

Sensilift Pro (ST300XXYYZZZ) received FDA 510(k) clearance on 2026-01-06, under 510(k) number K250341.

Who is the listed applicant for Sensilift Pro (ST300XXYYZZZ)?

The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sensilift Pro (ST300XXYYZZZ)?

The FDA product code for Sensilift Pro (ST300XXYYZZZ) is PAY.

Other records listing El Global Trade, Ltd. as applicant

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Related Devices (Code: PAY)

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.

K242227GENEO X ELITEPollogen, Ltd.K240616FAQ™ (102)Foreo, Inc.K233766Geneo X ElitePollogen, Ltd.K232424CurrentBody Skin RFEl Global Trade, Ltd.K230013Silk'n Titan AllwaysSilk'N Beauty , Ltd.K220322Pollogen STOP U Model UXV DevicePollogen, 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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