NailLift
K-Number: K230841 · 2024-01-22
Device Summary
NailLift is a medical device manufactured by Jps Corporation. It received FDA 510(k) clearance on 2024-01-22 under approval 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. It is manufactured by Jps Corporation. The 510(k) number is K230841.
When was NailLift approved by the FDA?
NailLift received FDA 510(k) clearance on 2024-01-22, under approval number K230841.
What company makes NailLift?
NailLift is manufactured by Jps Corporation.
What is the FDA product code for NailLift?
The FDA product code for NailLift is MQZ.
Related Devices (Code: MQZ)
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.