FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

NUVENTUS NV.C™ Prosthetic Components

K Number: K251220 · Decision Jul 28, 2025
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
3
Review Days
98

Basic Information

Device Name
NUVENTUS NV.C™ Prosthetic Components
K Number
K251220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Infinitum Eta, Ltd.
Date Received
April 21, 2025
Decision Date
July 28, 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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K Number Device Name
K243317 NUVENTUS NV.C™ Surgical Cassette and Tray
K233081 NUVENTUS NV.C™ Dental Implant System