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

Healing Abutment, Cover Screw

K Number: K210826 · Decision Feb 3, 2022
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
32
Review Days
321

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Healing Abutment, Cover Screw
K Number
K210826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Megagen Implant Co., Ltd.
Date Received
March 19, 2021
Decision Date
February 3, 2022
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.

View all

Other Clearances by Megagen Implant Co., Ltd.

K Number Device Name
K251232 MegaGen Zygoma Dental Implant System
K242030 MegaGen Dental Implant Abutment
K241972 BLUEDIAMOND IMPLANT
K234142 TiGEN Abutment, PMMA Abutment and Scan Healing Abutment
K240754 N2
K233450 MegaGen Dental Implant Abutment - Scan Healing Abutment; Temporary Abutment; Temporary Cylinder; Comfort Cap; Healing Cap; Healing Cap Screw; Milling Abutment; EZ Post Abutment; Extra EZ Post Abutment; EZ Post Cylinder; ZrGEN Abutment; Multi-unit Abutment; Multi-unit Angled Abutment; AXA Abutment (Straight); AXA Abutment (Angled); Abutment Screw; Cylinder Screw; Crown Screw
K231967 ARi ExCon Implant System
K223909 R2GATE Lite TM
K230618 MegaGen Dental Implant Systems Portfolio - MR Conditional
K223339 Bone Chamber Implant
Search all 32 clearances from Megagen Implant Co., Ltd. →