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

INSERTION TOOLS

K Number: K891617 · Decision May 1, 1989
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
18
Review Days
42

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Basic Information

Device Name
INSERTION TOOLS
K Number
K891617
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Implant Innovations International, Inc.
Date Received
March 20, 1989
Decision Date
May 1, 1989
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

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Other Clearances by Implant Innovations International, Inc.

K Number Device Name
K935544 3I STANDARD THREADED/SELF-TAPPING THREADED IMPLANTS MODIFICATION
K932123 IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM
K911655 IMPLARETTE
K905303 ABUTMENT GLO
K911701 G-FLOSS & G-FLOSS II
K891613 OVERDENTURE ATTACHMENT
K891612 DRILLING MACHINE W/HANDPIECES & INTERNAL IRRIGA.
K891618 TITANIUM FORCEPS
K891615 SURGICAL DRILLS
K874590 INNOVATIVE IMPLANTS AND COVER SCREWS
Search all 18 clearances from Implant Innovations International, Inc. →