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

Bone Screw

K Number: K251569 · Decision Aug 13, 2025
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
68
Review Days
83

Basic Information

Device Name
Bone Screw
K Number
K251569
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osstem Implant Co., Ltd.
Date Received
May 22, 2025
Decision Date
August 13, 2025
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZL), ordered by most recent decision date.

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Other Clearances by Osstem Implant Co., Ltd.

K Number Device Name
K251434 Healing Abutment System
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
K210097 Estar-Z
Search all 68 clearances from Osstem Implant Co., Ltd. →