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

Dentium NR Line CAD/CAM Abutments

K Number: K170384 · Decision Aug 17, 2017
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
22
Review Days
191

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Basic Information

Device Name
Dentium NR Line CAD/CAM Abutments
K Number
K170384
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentium Co., Ltd.
Date Received
February 7, 2017
Decision Date
August 17, 2017
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 Dentium Co., Ltd.

K Number Device Name
K213599 SuperLine
K193341 iCTmotor (WL-1)
K192436 Healing Abutments and Cover Screws
K191634 Scan Abutments and Comfort Caps
K172640 Dentium Implantium & SuperLine Prosthetics
K171622 Dentium Ti-Base
K171126 Implantium II
K160965 SuperLine
K161713 Dentium CAD/CAM Abutments
K160828 Dentium Implantium & SuperLine Prosthetics
Search all 22 clearances from Dentium Co., Ltd. →