FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

Elos Accurate® Denture Fixation System

K Number: K253774 · Decision May 20, 2026
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
13
Review Days
175

Basic Information

Device Name
Elos Accurate® Denture Fixation System
K Number
K253774
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elos Medtech Pinol A/S
Date Received
November 26, 2025
Decision Date
May 20, 2026
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 Elos Medtech Pinol A/S

K Number Device Name
K251497 Elos Accurate Hybrid Base
K242025 Elos Accurate® Hybrid Base™
K241722 Elos Accurate® Hybrid Base™; Elos Accurate® Customized Abutment
K231307 Elos Accurate Customized Abutment
K230317 Elos Accurate Hybrid Base
K222044 Elos Accurate Customized Abutment
K201860 Elos Accurate Hybrid Base
K191919 Elos Accurate Hybrid Base
K191890 Elos Accurate Customized Abutment
K192457 Elos Accurate Customized Abutment
Search all 13 clearances from Elos Medtech Pinol A/S →