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

FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS TPS COATING; FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS HA

K Number: K994376 · Decision Mar 24, 2000
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
18
Review Days
88

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Basic Information

Device Name
FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS TPS COATING; FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS HA
K Number
K994376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Friadent GmbH
Date Received
December 27, 1999
Decision Date
March 24, 2000
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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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
K023799 FRIOS ALGIPORE
K021318 XIVE DENTAL IMPLANT SYSTEM
Search all 18 clearances from Friadent GmbH →