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

FRIOS ALGIPORE

K Number: K023799 · Decision Feb 5, 2003
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
18
Review Days
83

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Basic Information

Device Name
FRIOS ALGIPORE
K Number
K023799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Friadent GmbH
Date Received
November 14, 2002
Decision Date
February 5, 2003
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

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Other Clearances by Friadent GmbH

K Number Device Name
K040170 FRIADENT PLUS DENTAL IMPLANT SYSTEMS
K041509 ANKYLOS DENTAL IMPLANT SYSTEM
K040946 ANKYLOS DENTAL IMPLANT SYSTEM
K032302 XIVE TG ABUTMENTS
K031674 MODIFICATION TO FRIALIT-2 DENTAL IMPLANT SYSTEM
K032158 XIVE DENTAL IMPLANT SYSTEM MULTIPLE
K032284 XIVE TG DENTAL IMPLANT SYSTEM
K024004 XIVE TRANSGINGIVAL DENTAL IMPLANT SYSTEM
K021318 XIVE DENTAL IMPLANT SYSTEM
K013067 FRIALOC DENTAL IMPLANT SYSTEM
Search all 18 clearances from Friadent GmbH →