FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Straumann® ProClean™ Cassette (041.800 ; 041.801)

K Number: K260726 · Decision Jun 3, 2026
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
90
Review Days
90

Basic Information

Device Name
Straumann® ProClean™ Cassette (041.800 ; 041.801)
K Number
K260726
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Institut Straumann AG
Date Received
March 5, 2026
Decision Date
June 3, 2026
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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