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

O.A.S.I. SYSTEM

K Number: K051552 · Decision Sep 19, 2005
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
98

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Basic Information

Device Name
O.A.S.I. SYSTEM
K Number
K051552
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lancer Orthodontics, Inc.
Date Received
June 13, 2005
Decision Date
September 19, 2005
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 Lancer Orthodontics, Inc.

K Number Device Name
K122069 STORM MINI SCREW
K071192 BLUGOO HD
K991481 PARAGON
K904090 ORTHODONTIC BONDING ADHESIVE CONTROL
K904092 LANCER ORIGINAL, SIERRA, GENERAL PURPOSE
K904093 BUCCAL TUBE, BUCCAL ATTACHMENT
K904091 TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO
K904089 PERMA MESH
K904094 C.A.T.,SINTERLINE,NATURAL ARCH,MICROTWIN,BIOTORQUE
K902075 INTRIGUE CERAMIC BRACKET
Search all 14 clearances from Lancer Orthodontics, Inc. →