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FDA 510(k)

NailLift

K-Number: K230841 · 2024-01-22

ApplicantJps Corporation
Decision Date2024-01-22
Product CodeMQZ
DecisionSubstantially Equivalent

Device Summary

NailLift is the device name listed in this FDA 510(k) record. The listed applicant is Jps Corporation. It received FDA 510(k) clearance on 2024-01-22 under 510(k) number K230841. The device is classified under product code MQZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NailLift?

NailLift is a medical device that received FDA 510(k) clearance on 2024-01-22. The listed applicant is Jps Corporation. The 510(k) number is K230841.

When did NailLift receive FDA 510(k) clearance?

NailLift received FDA 510(k) clearance on 2024-01-22, under 510(k) number K230841.

Who is the listed applicant for NailLift?

The FDA 510(k) record lists Jps Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NailLift?

The FDA product code for NailLift is MQZ.

Related Devices (Code: MQZ)

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.

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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.

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