FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇩 Andorra

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4

K Number: K010132 · Decision Jun 4, 2002
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
11
Review Days
504

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4
K Number
K010132
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SOADCO, S.L.
Date Received
January 16, 2001
Decision Date
June 4, 2002
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

Similar 510(k) Clearances

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

View all

Other Clearances by SOADCO, S.L.

K Number Device Name
K243128 Klockner Kits
K230103 Klockner Abutments
K173642 KLOCKNER SURGICAL BOX
K170022 Klockner Vega TiBase for CEREC
K153098 KLOCKNER VEGA DENTAL IMPLANT SYSTEM
K151194 KLOCKNER DENTAL IMPLANT ABUTMENTS (II)
K122988 KLOCKNER DENTAL IMPLANT ABUTMENTS
K082200 KLOCKNER ESSENTIAL DENTAL IMPLANTS SYSTEM, MODEL ESSENTIAL CONE 1.5
K080224 KLOCKNER ESSENTIAL DENTAL IMPLANTS SYSTEM, MODELS ESSENTIAL CONE (EC), ESSENTIAL SOLID (ES) AND ECK
K052654 KLOCKNER DENTAL IMPLANT, MODEL S3M
Search all 11 clearances from SOADCO, S.L. →