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FDA 510(k)

Plastic Surgical Kits

K-Number: K251300 · 2025-07-22

ApplicantDentsply Sirona, Inc.
Decision Date2025-07-22
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Plastic Surgical Kits is a medical device manufactured by Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2025-07-22 under approval number K251300. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Plastic Surgical Kits?

Plastic Surgical Kits is a medical device that received FDA 510(k) clearance on 2025-07-22. It is manufactured by Dentsply Sirona, Inc.. The 510(k) number is K251300.

When was Plastic Surgical Kits approved by the FDA?

Plastic Surgical Kits received FDA 510(k) clearance on 2025-07-22, under approval number K251300.

What company makes Plastic Surgical Kits?

Plastic Surgical Kits is manufactured by Dentsply Sirona, Inc..

What is the FDA product code for Plastic Surgical Kits?

The FDA product code for Plastic Surgical Kits is KCT.

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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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