510(k) K242564

Device
Autoclavable Cassette (Glidewell HT? Implant Guided Surgical Kit, Glidewell HT? Implant Surgical Kit, Glidewell? Prosthetic Kit)
Applicant
Prismatik Dentalcraft, Inc.
510(k) number
K242564
Product code
KCT
Decision
Substantially Equivalent (SESE)
Decision date
2025-03-21
Date received
2024-08-28
Regulation
880.6850
Classification name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Haiyan Wei
Address
2144 Michelson Dr. Irvine CA US 92612 92612

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KCT#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AG2026-06-03
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K251614Stainless Steel Surgical KitsDentsply Sirona, Inc.2026-02-06
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K251300Plastic Surgical KitsDentsply Sirona, Inc.2025-07-22
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K242762Aesculap Aicon® Series Container SystemAesculap, Inc.2025-05-13
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K241927Synthes Graphic Case & Tray SystemSynthes GmbH2025-03-28
K242023Microdent Sterilization CassetteImplant Microdent System S.L.U.2025-02-19
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K243128Klockner KitsSOADCO, S.L.2024-12-18