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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 the device name listed in this FDA 510(k) record. The listed applicant is Triworks Group Srl. It received FDA 510(k) clearance on 2022-07-07 under 510(k) 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. The listed applicant is Triworks Group Srl. The 510(k) number is K212472.

When did AgeJet receive FDA 510(k) clearance?

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

Who is the listed applicant for AgeJet?

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

What is the FDA product code for AgeJet?

The FDA product code for AgeJet is GEI.

Other records listing Triworks Group Srl as applicant

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.

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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