Plastic Surgical Kits
K-Number: K251300 · 2025-07-22
Device Summary
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. The listed applicant is Dentsply Sirona, Inc.. The 510(k) number is K251300.
When did Plastic Surgical Kits receive FDA 510(k) clearance?
Plastic Surgical Kits received FDA 510(k) clearance on 2025-07-22, under 510(k) number K251300.
Who is the listed applicant for Plastic Surgical Kits?
The FDA 510(k) record lists Dentsply Sirona, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Plastic Surgical Kits?
The FDA product code for Plastic Surgical Kits is KCT.
Other records listing Dentsply Sirona, Inc. 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.
Related Devices (Code: KCT)
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.
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.