FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

SIMDA Abutments

K Number: K252320 · Decision Dec 18, 2025
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
3
Review Days
146

Basic Information

Device Name
SIMDA Abutments
K Number
K252320
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Simda Co., Ltd.
Date Received
July 25, 2025
Decision Date
December 18, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NHA), ordered by most recent decision date.

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Other Clearances by Simda Co., Ltd.

K Number Device Name
K232271 SIMDA abutment
K223663 SIMDA Abutment