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

IMPLANT BODY DEPTH GAUGE/TRYIN

K Number: K946129 · Decision Mar 1, 1995
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
17
Review Days
75

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Basic Information

Device Name
IMPLANT BODY DEPTH GAUGE/TRYIN
K Number
K946129
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
O Co., Inc.
Date Received
December 16, 1994
Decision Date
March 1, 1995
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 O Co., Inc.

K Number Device Name
K033392 IMMEDIATE STABILIZING IMPLANT (ISI)
K023336 OCO DENTAL IMPLANT (5.0MM DIAMETER)
K021460 OCO DENTAL IMPLANT
K011524 IMMEDIATE STABILIZING DEVICE (ISD)
K010142 OCO DENTAL IMPLANT
K973926 O BUTMENT HS IMPLANT
K961665 O BUTMENT ET IMPLANT
K950066 DENTAL IMPLANT ENDOSSEOUS
K946113 IMPLANT BODY RETRIEVER/REMOVER
K945300 ACCESSORY ITEM TO ENDOSSEOUS DENTAL IMPLANT
Search all 17 clearances from O Co., Inc. →