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

MIS DENTAL IMPLANT SYSTEM

K Number: K040807 · Decision Jun 9, 2004
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
72

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Basic Information

Device Name
MIS DENTAL IMPLANT SYSTEM
K Number
K040807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mis - Implant Technologies , Ltd.
Date Received
March 29, 2004
Decision Date
June 9, 2004
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.

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Other Clearances by Mis - Implant Technologies , Ltd.

K Number Device Name
K103089 SEVEN IMPLANTS; BIOCOM IMPLANTS; LANCE IMPLANTS
K080458 MIS CREST WIDENER