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FDA 510(k)

EmbedMed

K-Number: K221943 · 2023-02-01

Applicant3D Lifeprints UK , Ltd.
Decision Date2023-02-01
Product CodePBF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EmbedMed is a medical device manufactured by 3D Lifeprints UK , Ltd.. It received FDA 510(k) clearance on 2023-02-01 under approval number K221943. The device is classified under product code PBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EmbedMed?

EmbedMed is a medical device that received FDA 510(k) clearance on 2023-02-01. It is manufactured by 3D Lifeprints UK , Ltd.. The 510(k) number is K221943.

When was EmbedMed approved by the FDA?

EmbedMed received FDA 510(k) clearance on 2023-02-01, under approval number K221943.

What company makes EmbedMed?

EmbedMed is manufactured by 3D Lifeprints UK , Ltd..

What is the FDA product code for EmbedMed?

The FDA product code for EmbedMed is PBF.

Other Devices by 3D Lifeprints UK , Ltd.

K220366EmbedMed

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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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