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FDA 510(k)

AgeJet

K-Number: K212472 · 2022-07-07

ApplicantTriworks Group Srl
Decision Date2022-07-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AgeJet is a medical device manufactured by Triworks Group Srl. It received FDA 510(k) clearance on 2022-07-07 under approval number K212472. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AgeJet?

AgeJet is a medical device that received FDA 510(k) clearance on 2022-07-07. It is manufactured by Triworks Group Srl. The 510(k) number is K212472.

When was AgeJet approved by the FDA?

AgeJet received FDA 510(k) clearance on 2022-07-07, under approval number K212472.

What company makes AgeJet?

AgeJet is manufactured by Triworks Group Srl.

What is the FDA product code for AgeJet?

The FDA product code for AgeJet is GEI.

Other Devices by Triworks Group Srl

K192621Medical RF

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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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