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

HySil Impression Materials

K Number: K181236 · Decision Sep 13, 2018
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
68
Review Days
126

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Basic Information

Device Name
HySil Impression Materials
K Number
K181236
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osstem Implant Co., Ltd.
Date Received
May 10, 2018
Decision Date
September 13, 2018
Product Code
ELW
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
ELW Material, Impression

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Other Clearances by Osstem Implant Co., Ltd.

K Number Device Name
K251434 Healing Abutment System
K251569 Bone Screw
K242521 Estar-ZE
K233806 T2 Plus
K233194 TS Abutment System
K232220 SS Abutment System
K232012 N1
K222778 Osstem Implant System
K221684 Osstem Abutment System
K212303 T2
Search all 68 clearances from Osstem Implant Co., Ltd. →