FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Atlantis® Abutments in Titanium

K Number: K252343 · Decision Dec 9, 2025
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
65
Review Days
134

Basic Information

Device Name
Atlantis® Abutments in Titanium
K Number
K252343
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
July 28, 2025
Decision Date
December 9, 2025
Product Code
NHA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NHA Abutment, Implant, Dental, Endosseous

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