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FDA 510(k)

Exceed Unlimited

K-Number: K233709 · 2024-02-23

ApplicantMt. Derm GmbH
Decision Date2024-02-23
Product CodeQAI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Exceed Unlimited is a medical device manufactured by Mt. Derm GmbH. It received FDA 510(k) clearance on 2024-02-23 under approval number K233709. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Exceed Unlimited?

Exceed Unlimited is a medical device that received FDA 510(k) clearance on 2024-02-23. It is manufactured by Mt. Derm GmbH. The 510(k) number is K233709.

When was Exceed Unlimited approved by the FDA?

Exceed Unlimited received FDA 510(k) clearance on 2024-02-23, under approval number K233709.

What company makes Exceed Unlimited?

Exceed Unlimited is manufactured by Mt. Derm GmbH.

What is the FDA product code for Exceed Unlimited?

The FDA product code for Exceed Unlimited is QAI.

Other Devices by Mt. Derm GmbH

K180778Exceed Microneedling Device K182407Exceed Microneedling device

Related Devices (Code: QAI)

K180778Exceed Microneedling DeviceMt. Derm GmbH DEN160029SkinPen Precision SystemBellus Medical, LLC K182407Exceed Microneedling deviceMt. Derm GmbH K200044SkinStylus SteriLock MicroSystemEsthetic Education, LLC K192138Rejuvapen NXTRefine USA, LLC K212558MicroPen EVOEclipse Medcorp, LLC

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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