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

HIOSSEN IMPLANT SYSTEM

K Number: K140934 · Decision Nov 12, 2014
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
13
Review Days
215

Basic Information

Device Name
HIOSSEN IMPLANT SYSTEM
K Number
K140934
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HIOSSEN INC.
Date Received
April 11, 2014
Decision Date
November 12, 2014
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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K123471 ETII SA FIXTURE SYSTEM
K123627 ET SMARTFIT ABUTMENT
K112532 ET II BIO-SA FIXTURE SYSTEM
K103537 ET III SA ULTRA WIDE SYSTEM
K101096 HT III SA FIXTURE SYSTEM
K093889 MODIFICATION TO: HG III ULTRA WIDE SYSTEM
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