FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OCO DENTAL IMPLANT

K Number: K010142 · Decision Feb 1, 2001
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
17
Review Days
15

Basic Information

Device Name
OCO DENTAL IMPLANT
K Number
K010142
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
O CO., INC.
Date Received
January 17, 2001
Decision Date
February 1, 2001
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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K021460 OCO DENTAL IMPLANT
K011524 IMMEDIATE STABILIZING DEVICE (ISD)
K973926 O BUTMENT HS IMPLANT
K961665 O BUTMENT ET IMPLANT
K950066 DENTAL IMPLANT ENDOSSEOUS
K946129 IMPLANT BODY DEPTH GAUGE/TRYIN
K946113 IMPLANT BODY RETRIEVER/REMOVER
K944904 PARRALLEL PIN
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